Relevant bibliographies by topics / Complex syndrome hypertension

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Complex syndrome hypertension'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Complex syndrome hypertension"

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Mishchuk, N. E. "Nocturnal hypertension syndrome in combination with orthostatic hypotension: a complex scenario in the treatment of hypertension." Medicine of Ukraine, no. 4(250) (June 16, 2021): 35–40. http://dx.doi.org/10.37987/1997-9894.2021.4(250).238122.

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One of the most difficult scenarios in the treatment of hypertension is the syndrome of neurogenic orthostatic hypotension - hypertension in the supine position.Despite the large number of observations, publications and even a number of randomized studies, this syndrome remains poorly known and often remains unrecognized. In this regard, in 2017, the recommendations of leading experts in the United States and Canada on screening, diagnosis and treatment of neurogenic orthostatic hypertension and associated hypertension in the supine position were published.The principles and features of the di
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Kamalov, I. I. "Radiological features of hypertension-hydrocephalus syndrome." Kazan medical journal 67, no. 4 (1986): 287–89. http://dx.doi.org/10.17816/kazmj70529.

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The aim of this work was to differentiate the signs of hypertension and hydrocephalus, analyze and systematize them. We carried out complex radiological study of 97 patients (67 males and 30 females) with hypertension and hydrocephalus syndrome aged 25-30 years old with the determination of pressure in the liquor system. Observations showed that hypertension (increase of cerebrospinal pressure) in 17 patients proceeded without hydrocephalus.
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Kohli, Utkarsh. "Shone’s complex in a patient with chromosome 9q34.3 deletion (Kleefstra syndrome)." Cardiology in the Young 29, no. 2 (2018): 249–51. http://dx.doi.org/10.1017/s104795111800210x.

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AbstractKleefstra syndrome (chromosome 9q34.3 deletion) is a rare genetic disorder with less than 110 patients reported till date. We report a 4-month-old Caucasian girl with Kleefstra syndrome and Shone’s complex, an association which has not been previously reported. Surgical planning for patients with Kleefstra syndrome and complex CHD can pose challenges due to an uncertain natural history and a risk of post-operative pulmonary hypertension.
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Ignatenko, Grigory A., Ilya S. Grekov, Marina V. Grushina, and Anna V. Dubovyk. "A complex case of diagnosis of Conn’s syndrome." I.P. Pavlov Russian Medical Biological Herald 28, no. 1 (2020): 67–72. http://dx.doi.org/10.23888/pavlovj202028167-72.

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The primary hyperaldosteronism also known as Conns syndrome, is a rarely diagnosed disease that commonly runs under a mask of ischemic heart disease and the primary arteria hypertension (AH). Nevertheless, the incidence of the given pathology among all patients with AH makes almost 17%. On the other hand, the absence of specific clinical manifestations of the disease makes its timely and correct diagnosis difficult which is fraught with serious complications. In the article a clinical case of Conns syndrome and peculiarities of its diagnosis are described.
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Lozhkina, N. G., and A. N. Spiridonov. "Clinical case: early connection of valsartan/sacubitril in the treatment of hypertension." Kardiologiia 62, no. 5 (2022): 72–74. http://dx.doi.org/10.18087/cardio.2022.5.n1977.

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Metabolic syndrome is a disease the World Health Organization has called a new pandemic of the 21st century. Arterial hypertension is one of the criteria for this diagnosis and a determinant of damage to major target organs. The present clinical case demonstrates an experience of treatment of arterial hypertension associated with metabolic syndrome with a valsartan/sacubitril molecular complex.
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Akhundova, Maleyka, and Sabina Majidova. "HEERFORDT-WALDENSTRÖM SYNDROME (CLINICAL CASE)." Azerbaijan Journal of Ophthalmology, no. 2025/17/01/52 (April 8, 2025): 71–79. https://doi.org/10.71110/ajo791020251701527179.

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The article presents a clinical case of Heerfordt-Waldenström syndrome of patient A.Sh., born in 1972, who was undergoing inpatient treatment at the National Ophthalmology Centre named after Academician Zarifa Aliyeva. This syndrome manifested itself as anterior uveitis, facial nerve paralysis and of bilateral parotitis in anamnesis. Based on specific and ophthalmological examination, the following diagnosis was made: “Sarcoidosis, Heerfordt-Waldenström syndrome, uveitis, uveitic ocular hypertension of the right eye”. Appropriate complex therapy was carried out and a positive result was obtain
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Paykova, Alexandra S., Michail V. Alexandrov та Svetlana E. Ushakova. "The Еffectiveness of Stabilometrical Training in the Complex of Rehabilitation Measures in Elderly and Senile Patients with Arterial Hypertension". Bulletin of Rehabilitation Medicine 20, № 3 (2021): 53–58. http://dx.doi.org/10.38025/2078-1962-2021-20-3-53-58.

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The treatment and rehabilitation of elderly patients with hypertension is often hampered by their existing geriatric syndromes of senileasthenia and the risk of falls. Stabilometric balance training will allow to maintain the level of physical functioning and supporting theautonomy of this category of patients. Aim. To assess the possibilities of using stabilometric training with biofeedback to correct the risk of falls in patients aged 63 and olderwith arterial hypertension. Material and methods. On the basis of the geriatric department of the Regional Budgetary Institution of Health «Ivanovo
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Corredor-Orlandelli, David, Camila Borda, Juan Sebastian Sierra, and Daniel Gerardo Fernández-Ávila. "Multiple-autoimmune syndrome causing interstitial lung disease in the presence of pulmonary hypertension and Erasmus syndrome." Rheumatology (Bulgaria) 31, no. 4 (2024): 123–28. http://dx.doi.org/10.35465/31.4.2023.pp123-128.

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Connective tissue diseases constitute a group of inflammatory disorders that can concurrently affect multiple organs. Pulmonary manifestations of connective tissue diseases include interstitial lung disease, pulmonary hypertension, pleural diseases, and airway compromise. Both interstitial lung disease and pulmonary arterial hypertension have high morbidity and mortality in these patients. Interstitial lung disease affects 40 % - 50 % of patients with connective tissue diseases, predominantly systemic sclerosis, rheumatoid arthritis, and inflammatory myopathies. Parenchymal compromise is heter
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Ng, Wei Wei, and Shanty Velaiutham. "CARNEY COMPLEX." Journal of the ASEAN Federation of Endocrine Societies 39, S1 (2024): 22–23. https://doi.org/10.15605/jafes.039.s1.032.

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INTRODUCTION/BACKGROUND Carney complex (CNC) is a rare multiple endocrine neoplasia characterized by spotty skin pigmentation, myxomas and endocrine overactivity. We report a case of a young female with multiple typical manifestations of CNC over the past 12 years, including bilateral primary pigmented nodular adrenocortical disease, bilateral breast ductal adenoma, cardiac myxoma and thyroid nodule. CASEThis female first presented at age 28 for secondary amenorrhea, weight gain and uncontrolled hypertension. She had pigmentation over her lips and features of Cushing syndrome, such as facial p
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De Laura, D., V. Lavolpe, D. Rutigliano, et al. "P392 POST–THROMBOEMBOLIC PULMONARY HYPERTENSION: A COMPLEX CASE." European Heart Journal Supplements 25, Supplement_D (2023): D198. http://dx.doi.org/10.1093/eurheartjsupp/suad111.463.

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Abstract Introduction Patients with post–thromboembolic pulmonary hypertension (CTEPH) achieve functional recovery after pulmonary endarterectomy (PEA). 40% of them are inoperable (1,2). Clinical case 66–year–old man admitted in 2012 to our ward for dyspnea on exertion and high echocardiographic probability of pulmonary hypertension (PI). Medical history: smoking; thalassemia trait; COPD; splenectomy at 13; diagnosis of chronic myeloproliferative syndrome. BP: 120/70 mmHg. NYHA class III. Blood tests: Hb: 9.4 g/dl; MCV: 70; HCT: 30%; PLT: 511; WBC: 14.84 (Mo 13%).NT–pro BNP:933. Autoantibodies
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Dissertations / Theses on the topic "Complex syndrome hypertension"

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Xu, Hai. "Structural Modeling and Analysis of Structures in Aorta Images." Thesis, 2011. http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-9779.

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Morphology change analysis of aorta images acquired from biological experiments plays a critical role in exploring the relationship between lamina thickness (LT), interlamellar distance (ILD) and fragmentation (furcation points) with respect to pathological conditions. An automated software tool now is available to extract elastic laminae (EL) and measure LT, ILD and fragmentation along their ridge lines in a fine detailed aspect. A statistical randomized complete block design (RCBD) and F-test were used to assess potential (non)-uniformity of LT and ILD along both radial and circumferential d
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Books on the topic "Complex syndrome hypertension"

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Bissell, Lesley-Anne, Dwomoa Adu, and Paul Emery. The patient with rheumatoid arthritis, mixed connective tissue disease, Sjögren syndrome, or polymyositis. Edited by Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0166.

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Renal disease is a well-recognized cause of ill health and death in rheumatoid arthritis. Three broad categories of renal disease occur. The first—and by far the most common—arises from the nephrotoxicity of the drugs used in the treatment of arthritis, particularly with non-steroidal anti-inflammatory drugs. Disease-modifying antirheumatic drugs such as gold and D-penicillamine may lead to proteinuria and a glomerulonephritis in 10–30% of patients. Ciclosporin is associated with significant nephrotoxicity and hypertension. A second major but diminishing cause of renal disease in rheumatoid ar
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Waldmann, Carl, Neil Soni, and Andrew Rhodes. Obstetric emergencies. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199229581.003.0031.

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Pre-eclampsia 518Eclampsia 520HELLP syndrome 522Postpartum haemorrhage 524Amniotic fluid embolism 526Pre-eclampsia is a common complication of pregnancy, UK incidence is 3–5%, with a complex hereditary, immunological and environmental aetiology.Abnormal placentation is characterized by impaired myometrial spiral artery relaxation, failure of trophoblastic invasion of these arterial walls and blockage of some vessels with fibrin, platelets and lipid-laden macrophages. There is a 30–40%, reduction in placental perfusion by the uterine arcuate arteries as seen by Doppler studies at 18–24 weeks ge
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Rodríguez-Iturbe, Bernardo, and Mark Haas. Post-streptococcal glomerulonephritis. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0077_update_001.

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Post-streptococcal glomerulonephritis is a complication of Streptococcal infections that is responsible for classic acute nephritic syndrome, mostly seen in children. This is an acute nephritis associated with prominent fluid retention and oedema, hypertension and haematuria. Serum complement levels are diagnostically helpful as C3 levels are characteristically very low. However, many cases are much less severe and may pass unrecognized, only being identified by screening for dipstick haematuria. In children recovery is the rule but in adults, often with comorbid conditions, the prognosis is s
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Ellinson, Michelle, and Tommy Rampling. Normal nutritional function. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0331.

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Normal nutritional function requires a healthy diet. Healthy eating incorporates a variety of nutrients that are essential for energy expenditure, prevention of disease, and maintenance of normal physiological function. An unhealthy diet can result in malnutrition, and this contributes to illness and death throughout the world. The core principle of healthy eating is obtaining an adequate balance, and the diseases resulting from overnourishment differ greatly from those resulting from undernourishment. In the third world, diets tend to rely heavily on staple crops, and can be very seasonal. En
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Book chapters on the topic "Complex syndrome hypertension"

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Malhotra, Ajai K. "Abdominal Compartment Syndrome and Hypertension in Patients Undergoing Abdominal Wall Reconstruction." In Surgery of Complex Abdominal Wall Defects. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55868-4_22.

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Malhotra, Ajai K. "Abdominal Compartment Syndrome and Hypertension in Patients Undergoing Abdominal Wall Reconstruction." In Surgery of Complex Abdominal Wall Defects. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-6354-2_21.

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Parikh, Garvita, Ramesh K. Goyal, and Bhoomika Patel. "Connecting the Dots: The Complex Relationship Between Metabolic Syndrome and Hypertension." In Advances in Biochemistry in Health and Disease. Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-75686-3_5.

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Burke, Frances, and Philippe Szapary. "Dyslipidemia, Hypertension and Metabolic Syndrome." In The Complete Guide to Nutrition in Primary Care. Blackwell Publishing Ltd, 2008. http://dx.doi.org/10.1002/9780470691793.ch7.

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Ehret, Georg. "Complex cardiovascular diseases: the genetics of arterial hypertension." In ESC CardioMed. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0166.

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Arterial hypertension appears as two genetic types: primary hypertension is to a substantial extent determined by a large number of genetic risk variants, whereas rare patients with a familial hypertensive syndrome have a single gene defect that drives the elevated blood pressure. The familial hypertensive syndromes have been instrumental in highlighting blood pressure-regulating pathways that almost exclusively cluster in the kidney and in the mineralocorticoid pathways. Conversely, hundreds or more genetic variants cause the genetic component of primary hypertension and each risk variant cau
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"Paediatric pulmonary hypertension." In Paediatric Cardiology, edited by Thomas Day, Aaron Bell, Sadia Quyam, and John Simpson. Oxford University PressOxford, 2024. http://dx.doi.org/10.1093/med/9780198863908.003.0012.

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Abstract Paediatric pulmonary hypertension is a complex topic, but has important implications for almost all aspects of paediatric cardiac care. This chapter includes an overview of pulmonary hypertension, including clinical approach and treatment. It also includes sections on the main subtypes of pulmonary hypertension, including Eisenmenger syndrome.
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Mulè, Massimiliano, Giulia Passaniti, and Daniela Giannazzo. "Pulmonary Hypertension." In Cardiovascular Diseases [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.107281.

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Pulmonary hypertension (PH) is a complex and multifactorial syndrome, partly unknown, characterized by a profound alteration of pulmonary vasculature and, consequentially, a rise in the pulmonary vascular load, leading to hypertrophy and remodeling of the right heart chambers. The World Health Organization assembles the several forms of PH into five clinical groups: group 1 includes pulmonary arterial hypertension, previously defined as idiopathic forms, group 2 is PH due to left-sided heart diseases, group 3 PH due to lung diseases, hypoxia, or both, group 4 due to pulmonary-artery obstructio
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Fatma Köksal Çakırlar. "Microbiota and Metabolic Syndrome." In Metabolic Syndrome: A Comprehensive Update with New Insights. BENTHAM SCIENCE PUBLISHERS, 2025. https://doi.org/10.2174/9789815322132125010020.

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Composed of trillions of microorganisms, the human GutM plays a key role in maintaining general health and metabolic homeostasis. MetS is a complex and common health condition characterized by a number of metabolic abnormalities, including obesity, insulin resistance, hypertension, and dyslipidemia. Evidence emerging in recent years indicates that human GutM plays a crucial role in the pathophysiology of MetS. In this chapter, we will discuss the composition and functionality of GutM, as well as the dynamic and complex relationship between GutM's influence on metS development and progression.
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Woods, Brian. "Abdominal Compartment Syndrome." In Critical Care. Oxford University PressNew York, 2022. http://dx.doi.org/10.1093/med/9780190885939.003.0027.

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Abstract Intra-abdominal hypertension (IAH) with new organ injury defines abdominal compartment syndrome (ACS). Common phenomena among the critically ill, IAH and ACS result from a wide range of medical and surgical disorders. ACS has devastating effects on multiple organ systems but is underrecognized with often misunderstood management. Complex interactions between the abdominopelvic organs, the chest, the cardiovascular, and the central nervous system occur with pathologic increases of abdominal pressure. Physical exam and usual measures of perfusion or hemodynamics require careful interpre
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L. Knop, Gustavo, and Alejandra Castro-Varela. "Double Lung and Heart-Lung Transplantation for Congenital Heart Disease with Eisenmenger Syndrome and Idiopathic Pulmonary Arterial Hypertension." In New Insights on Pulmonary Hypertension [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.1002214.

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Patients with pulmonary hypertension who develop concomitant refractory end-stage lung disease and/or chronic end-stage heart disease should undergo evaluation to determine if they are candidates for double lung (DLTx) or heart-lung transplantation (HLTx). Pulmonary hypertension is the indication for approximately 4.5% of total lung transplants. The most common indication for HLTx is complex congenital heart disease (CHD) with Eisenmenger syndrome. HLTx is also indicated in patients with idiopathic pulmonary arterial hypertension and severe right ventricular (RV) failure. Patients with pulmona
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Conference papers on the topic "Complex syndrome hypertension"

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Viégas, Jéssica de Vasconcelos Oliveira, Tainá Rodrigues Toqueton, Délio Guerra Drummond Júnior, et al. "Clinical treatment of metabolic syndrome in pregnant women." In II SEVEN INTERNATIONAL MEDICAL AND NURSING CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/iicongressmedicalnursing-022.

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Metabolic syndrome is a medical condition characterized by a set of cardiovascular risk factors, including obesity, hypertension, insulin resistance, and dyslipidemia. During pregnancy, a woman's body undergoes complex metabolic and hormonal changes to facilitate fetal development. However, when the pregnant woman has metabolic syndrome, these changes can be exacerbated, increasing the risk of serious obstetric complications and having a potential impact on maternal-fetal health.
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Nesović Ostojić, Jelena, Sanjin Kovačević, Nikola Mitović, Aleksandra Nenadović, Andrija Vuković, and Mirjana Jovanović. "When, how, and why is it necessary to assess kidney function in cardiovascular patients?" In 7th International Congress of Cardionephrology KARNEF 2025. Punta Niš, 2025. https://doi.org/10.46793/karnef25.182no.

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Renal function is an important aspect to evaluate in cardiovascular patients because kidney function and heart function are closely interconnected. Cardiorenal syndrome refers to this complex relationship, where either heart or kidney dysfunction can lead to worsening of the other, making their management more complex and challenging. Renal function in cardiovascular patietns should be assessed at the time of diagnosis of cardiovascular conditions (e.g., heart failure, coronary artery disease, or hypertension), as kidney function can impact the treatment plan and prognosis; during hospitalizat
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Ribeiro, Laíse Alves, João Victor Monteiro de Camargo, Bruno Buzá Joioso, and Ailton Joioso. "Metabolic syndrome as a risk factor for the development of breast cancer in women and its impact on prognosis." In Brazilian Breast Cancer Symposium 2023. Mastology, 2023. http://dx.doi.org/10.29289/259453942023v33s1086.

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Objective: Metabolic syndrome (MS) is a complex metabolic disorder. The aforementioned main components are systemic arterial hypertension, insulin resistance, obesity, and dyslipidemia. Highly acclaimed evidence supports the hypothesis that MS may be associated with breast cancer (BC) development and worse prognosis. The increasing incidence rates of both MS and BC seem to corroborate this theory. This article aims to assess the association between MS and BC development, later diagnosis, and worse prognosis. Methodology: An inclusive literature review was conducted on PubMed and SciELO. Result
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Martinelli, Jose, Jessica Ivanovs, and Marcos Martinelli. "GERIATRIC EVALUATION IN 27 CASES OF MUSICAL HALLUCINATION." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda073.

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Background: Musical hallucination (AM) is a type of complex auditory hallucination described as hearing musical tones, rhythms, harmonies, and melodies without the corresponding external auditory stimulus. This type of hallucination is relatively rare and is seen less often than other types of hallucination. Such hallucinations can be continuous or intermittent and are usually accompanied by a clear and critical awareness on the part of the patient. AM are found mainly in elderly women with progressive hearing loss, usually due to ear diseases or lesions. They also occur in neurological disord
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Walshe, K., I. Mackie, M. Gallimore, and S. J. Machin. "PERTURBATION OF THE KALLIKREIN-KININ SYSTEM IN ADULT RESPIRATORY DISTRESS SYNDROME (ARDS)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644336.

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Platelet and fibrin deposition in the small blood vessels of the lung as well as activation of the contact system with consequent kinin generation have been described in ARDS. It is thought that these haemostatic changes may play a role in the pathogenesis of the disease which include dyspnoea, hypoxaemia, pulmonary oedema, and pulmonary hypertension. We have studied a complete battery of tests for the proteases and inhibitors of the kallikrein-kinin system in an ongoing study of ARDS and haemostasis. 12 patients have so far been studied, with the following factors complicating ARDS: 5 had sep
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Barreira, Raphael Palomo, Vanessa Moraes Rossette, Thomas Zurga Markus Torres, et al. "Syndrome of one and middle of the vertical look: possible clinical entity associated with percheron artery ischemia: semiological and neuroanatomic aspects." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.467.

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Context: The acute paralysis of the vertical gaze is usually caused by a mesencephalic lesion because the control of the vertical conjugated gaze is found there; there are three main structures: the rostral interstitial nucleus of the medial longitudinal fascicle (riFLM), the Cajal interstitial nucleus and the posterior commissure (CP). The riFLM, contains burst neurons responsible for the saccades, projecting to the subnuclei of the upper rectum and inferior oblique to look upwards and subnuclei of the lower rectum and superior oblique to look downwards. The projections for the elevators appe
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Castro, Kaline dos Santos Kishishita, Amanda Alves Cardoso da Silva, Ana Clara Mota Gonçalo, et al. "SARS-CoV-2 and neurology: characteristics of patients with Covid-19 affected by CVA." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.085.

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Introduction: Since the beginning of the pandemic in December 2019, COVID-19 caused by the infection of the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2), in addition to the clinical manifestations already, can develop changes in the rate of blood clotting, where there are already notifications of Cerebrovascular Accident (CVA) associated with the virus. Objective: To know the characteristics of patients with COVID-19 affected by CVA, documented in the scientific literature. Method: A systematic literature review was carried out, using the MeSH Brower platform descriptors, namel
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Froio, Nayara de Lima, Ana Luisa Rosas Sarmento, Sonia Maria Cesar de Azevedo Silva, and Lilia Azzi Collet da Rocha Camargo. "Atypical Manifestation of Polyneuropathy in Covid-19." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.312.

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Context: Neurological manifestations of Sars-CoV-2 are progressively emerging. Cases of Guillain-Barré syndrome and its variants, with onset about 5-10 days after influenza symptoms, have been described. This paper reports a case of polyneuropathy with onset 90 days after a sore throat episode and persistence of IgM positivity in serology for Sars- Cov-2. We aim to raise awareness of this possibility. Case Report: A 56-year-old male, hypertensive, presented with sore throat on April 21, 2020. Serology for Covid-19 was performed with positive IgM. There was complete improvement of the symptom.
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Poton, André Rodrigues, Ana Carolina Andorinho de Freitas Ferreira, Leila Delorme Goldschmidt, Maria Fiorot Dalla, Barbara França Amorim, and Cristiane Borges Patroclo. "Introduction: The association of depressive and apathetic symptoms after lesions in the frontal region in the territory of the anterior cerebral artery is described, presumably due to interruption of complex subcortical frontal circuits. Objectives: Illustrate and discuss a bilateral frontal syndrome resulting from stroke in the territory of the anterior cerebral artery, as well as, the possible confusion between functional and organic conditions presenting the same symptoms. Results: 61-year-old man complaining of falls and left lower limb weakness. Moreover, had been interned due to suicide attempt recently. He is hypertensive and was addicted to alcohol and illicit drugs. Two years before, he had a left anterior cerebral artery ischemic that led to right lower limb paresis. At admission, he had poor interaction and presented hyperreflexia and Babinski sign at the right lower limb while normoreflexia at left. Computed tomography (CT) of the skull showed left frontal encephalomalacia. It was discarded metabolic and infectious disturbance as well as no signs of trauma from reported falls or high-risk lesions for new stroke. Psychiatric evaluations identified depression related to social, and economic factors. Pharmacological and behavioral measures were instituted. However, the condition worsened with the onset of mutism, akinesia, and abulia, which was attributed to the wors ening of depression. Antidepressant regimen was adjusted again and new brain CT was performed. It disclosed a new stroke of the right anterior cerebral artery. Initially, the symptoms were attributed to a functional condition and no organic justification was found. Nevertheless, the worsening of the basal status evolved to a catatonic manifestation, in parallel to a new frontal stroke. Previous contralateral frontal stroke might have turned the patient vulnerable to this condition. Nonetheless, the course of time eased by pharmacological strategy used (lithium, amitriptyline, and risperidone), was able to reverse the condition, except for left leg monoplegia evidenced after the restoration of spontaneous motricity. Conclusion: The case illustrates the clinical-anatomical correlations of anterior cerebral artery stroke, but also highlights the interface between neurology and psychiatry." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.787.

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Introduction: The association of depressive and apathetic symptoms after lesions in the frontal region in the territory of the anterior cerebral artery is described, presumably due to interruption of complex subcortical frontal circuits. Objectives: Illustrate and discuss a bilateral frontal syndrome resulting from stroke in the territory of the anterior cerebral artery, as well as, the possible confusion between functional and organic conditions presenting the same symptoms. Results: 61-year-old man complaining of falls and left lower limb weakness. Moreover, had been interned due to suicide
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Reports on the topic "Complex syndrome hypertension"

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Wideman, Jr., Robert F., Nicholas B. Anthony, Avigdor Cahaner, Alan Shlosberg, Michel Bellaiche, and William B. Roush. Integrated Approach to Evaluating Inherited Predictors of Resistance to Pulmonary Hypertension Syndrome (Ascites) in Fast Growing Broiler Chickens. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7575287.bard.

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Background PHS (pulmonary hypertension syndrome, ascites syndrome) is a serious cause of loss in the broiler industry, and is a prime example of an undesirable side effect of successful genetic development that may be deleteriously manifested by factors in the environment of growing broilers. Basically, continuous and pinpointed selection for rapid growth in broilers has led to higher oxygen demand and consequently to more frequent manifestation of an inherent potential cardiopulmonary incapability to sufficiently oxygenate the arterial blood. The multifaceted causes and modifiers of PHS make
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