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Artykuły w czasopismach na temat „Takayasu’s arteritis in children”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Saatova, G., A. Furtikova, R. Almazbekova, A. Asan kyzy, A. Matkasymova, and B. Zhanturaeva. "Nonspecific Aortoarteritis (Takayasu’s Arteritis) in Children: A Description of Cases at the New Coronavirus Infection COVID-19." Bulletin of Science and Practice 7, no. 11 (2021): 153–69. http://dx.doi.org/10.33619/2414-2948/72/20.

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A description of two cases of the Takayasu’s arteritis in children, who were under our observation, enrolled in the Department of Cardiology and Rheumatology of the National Center Maternity and Childhood Protection during the pandemic period of the new coronavirus infection in 2021 were presented. The Takayasu’s arteritis should be included in the structure of the differential diagnosis in children and adolescents with clinical manifestations characteristic of post-COVID syndrome.

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2

de Ranieri, Deirdre. "Great Vessels of Children: Takayasu’s Arteritis." Pediatric Annals 44, no. 6 (2015): e148-e152. http://dx.doi.org/10.3928/00904481-20150611-10.

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Lamichhane, Reshma Dhakal, and Ram Hari Chapagain. "Takayasu’s Arteritis: Rare Cause of Hypertension in Children." Journal of Nepal Paediatric Society 38, no. 2 (2019): 140–42. http://dx.doi.org/10.3126/jnps.v38i2.20551.

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Takayasu arteritis (TA) is a large vessel vasculitis that involves the aorta, its major branches and pulmonary arteries. Diagnosis of TA during childhood remains challenging due to the non-specific symptoms. We report a six years age boy with unresolved hypertension who was later diagnosed as childhood TA. Oral corticosteroid was started 2mg/kg/day. TA is rare in children; Childhood TA must be considered in children who present with, hypertension and increased acute phase reactants.

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4

Cilliers, Antoinette M., Paul E. Adams, Hopewell Ntsinjana, and Udai Kala. "Review of children with Takayasu’s arteritis at a Southern African tertiary care centre." Cardiology in the Young 28, no. 9 (2018): 1129–35. http://dx.doi.org/10.1017/s1047951118000938.

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AbstractIntroductionTakayasu’s arteritis is a rare idiopathic arteritis causing stenosis or aneurysms of the aorta, pulmonary arteries, and their branches. It usually occurs in women, but has been described in children.ObjectiveThe objective of this study was to determine the clinical presentation, demographic profile, vascular involvement, origins, management, and outcome of children diagnosed with Takayasu’s arteritis at a Southern African tertiary care centre between 1993 and 2015.MethodsThis is a retrospective analysis of all children with Takayasu’s arteritis captured on a computerised el

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5

Al abrawi, Safia, Marine Fouillet-Desjonqueres, Louis David, Xavier Barral, Pierre Cochat, and Rolando Cimaz. "Takayasu arteritis in children." Pediatric Rheumatology 6, no. 1 (2008): 17. http://dx.doi.org/10.1186/1546-0096-6-17.

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Halaweish, Ihab, Himanshu Patel, and Ming-Sing Si. "Giant aortic aneurysm in a child with Takayasu arteritis." Cardiology in the Young 26, no. 3 (2015): 593–95. http://dx.doi.org/10.1017/s1047951115001511.

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AbstractTakayasu arteritis is a chronic, idiopathic, granulomatous vasculitis involving the aorta, its major branches, and occasionally the pulmonary arteries. Although rare in children, it is the third most common vasculitis in the paediatric population. Although aneurysmal disease has been reported in adults with Takayasu arteritis, it is a rare entity in children. We present the case of a 10-year-old boy with a giant ascending and arch aneurysm that necessitated follow-up surgery for a new aneurysm and occlusive disease. This is also the first published case involving endovascular aortic gr

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7

Sönmez, Hafize Emine, Ferhat Demir, Semanur Özdel, et al. "Neuroimaging of Children With Takayasu Arteritis." Journal of Child Neurology 36, no. 8 (2021): 642–47. http://dx.doi.org/10.1177/0883073821991287.

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Objective: Takayasu arteritis is a rare granulomatous chronic vasculitis that affects the aorta and its main branches. Neurologic manifestations can accompany the disease; however, there is no study on neuroimaging in children with Takayasu arteritis. Therefore, we aimed to evaluate cranial magnetic resonance imaging (MRI) in pediatric Takayasu arteritis patients. Materials and Methods: Demographic, clinical, and laboratory data were obtained retrospectively. Results: The study included 15 pediatric Takayasu arteritis patients. All patients presented with constitutional symptoms. Additionally,

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8

Sgouropoulou, Vasiliki, Efthymia Vargiami, Maria Kyriazi, et al. "Recurrent Stroke as a Presenting Feature of Takayasu Arteritis in an Adolescent: A Case Report and Literature Review." Prague Medical Report 125, no. 1 (2024): 62–68. http://dx.doi.org/10.14712/23362936.2024.6.

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Takayasu arteritis is a large vessel vasculitis, characterized by granulomatous inflammation of arterial vessels, that typically affects the aorta, its main branches and pulmonary arteries. Disease diagnosis is a challenge and requires awareness of the condition, as clinical signs can be not specific. We report a case of an adolescent with recurrent stroke diagnosed with Takayasu arteritis. A diagnosis of Takayasu arteritis was established due to angiographic findings in the magnetic resonance angiography in conjunction with systolic blood pressure discrepancy, arterial hypertension and increa

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9

Bolek, Ertugrul Cagri, Ummusen Kaya Akca, Alper Sari, et al. "Is Takayasu's arteritis more severe in children?" Clinical and Experimental Rheumatology 39, no. 2 (2021): 32–38. http://dx.doi.org/10.55563/clinexprheumatol/kr357t.

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10

Brunner, J., B. M. Feldman, P. N. Tyrrell, et al. "Takayasu arteritis in children and adolescents." Rheumatology 49, no. 10 (2010): 1806–14. http://dx.doi.org/10.1093/rheumatology/keq167.

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11

Van Elburg, R. M., E. L. Henar, C. M. A. Bijleveld, T. R. Prins, and H. S. A. Heymans. "Vascular Compromise Prior to Intestinal Manifestations of Crohn's Disease in a 14‐Year‐Old Girl." Journal of Pediatric Gastroenterology and Nutrition 14, no. 1 (1992): 97–100. http://dx.doi.org/10.1002/j.1536-4801.1992.tb10498.x.

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SummaryVascular manifestations as extraintestinal symptoms of Crohn's disease are rare and only occasionally reported in children. A 14‐year‐old girl with vascular compromise prior to intestinal manifestations of Crohn's disease is described. The vascular symptoms were due to segmental narrowing of several major arteries as shown by angiography. This kind of vascular involvement in our patient is different from the pattern described in Crohn's disease and resembles Takayasu's disease. Recently, it has been suggested that Crohn's disease could be mediated by multifocal gastrointestinal infarcti

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12

Lyskina, G. A., V. A. Podzolkova, O. V. Shpitonkova, and Yu O. Kostina. "ISSUES IN SURGICAL TREATMENT OF CHILDREN WITH TAKAYASU’S ARTERITIS FROM THE PEDIATRIC PHYSICIAN’S POINT OF VIEW." Pediatria. Journal named after G.N. Speransky 101, no. 4 (2022): 137–45. http://dx.doi.org/10.24110/0031-403x-2022-101-4-137-145.

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The purposes of the study were as follows: to perform a comparative analysis of demographic and clinical data in children with Takayasu's arteritis (TA) who underwent surgical treatment of the underlying disease, to determine approaches to surgical interventions and to evaluate its outcomes. Materials and methods of the research: 51 children (boys:girls ratio 1:4.7) aged from 8 months till 17 years old (11 [9; 14] years as median) with a reliable TA diagnosis were observed from February, 2001 till January, 2022. The median age of the TA debut was 11 [9; 14] years. The single-center (I.M. Seche

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13

Obiagwu, Patience Ngozi, Priya Gajjar, Mignon McCulloch, Christian Scott, Alp Numanoglu, and Peter Nourse. "Salvageability of renal function following renal revascularisation in children with Takayasu’s arteritis-induced renal artery stenosis." South African Medical Journal 106, no. 8 (2016): 813. http://dx.doi.org/10.7196/samj.2016.v106i8.10490.

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Lyskina, G. A., and Y. O. Kostina. "MODERN ASPECTS OF NONSPECIFIC AORTOARTERITIS (TAKAYASU’S ARTERITIS) TREATMENT ANALYSIS OF BASIC THERAPY OPTIONS EFFICACY IN CHILDREN." Pediatria. Journal named after G.N. Speransky 96, no. 3 (2017): 86–93. http://dx.doi.org/10.24110/0031-403x-2017-96-3-86-93.

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15

Gaballah, Marian, Rachelle Goldfisher, and John B. Amodio. "The Utility of MRI in the Diagnosis of Takayasu Arteritis." Case Reports in Pediatrics 2017 (2017): 1–4. http://dx.doi.org/10.1155/2017/7976165.

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Takayasu Arteritis (TA) is an inflammatory disorder involving the thoracoabdominal aorta and its branches and the pulmonary arteries, with eventual vascular stenosis, occlusion, or aneurysm formation. Conventional angiography has been the reference imaging standard for diagnosis of TA. The purpose of this case report is to demonstrate the utility of MR imaging and MR angiography in the diagnosis of Takayasu Arteritis in a pediatric patient. The patient is a 15-year-old female patient presenting with anemia, hypertension, and acute kidney injury. Initial chest CT demonstrated ectasia of the asc

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16

Kalangos, Afksendiyos, Jan T. Christenson, Mustafa Cikirikcioglu, et al. "Long-term outcome after surgical intervention and interventional procedures for the management of Takayasu’s arteritis in children." Journal of Thoracic and Cardiovascular Surgery 132, no. 3 (2006): 656–64. http://dx.doi.org/10.1016/j.jtcvs.2006.04.020.

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17

McCulloch, Mignon, Savvas Andronikou, Elizabeth Goddard, et al. "Angiographic features of 26 children with Takayasu's arteritis." Pediatric Radiology 33, no. 4 (2003): 230–35. http://dx.doi.org/10.1007/s00247-002-0817-1.

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18

Sharma, Sandiv, Mira Rajani, Savitri Shrivastava, et al. "Non-specific aorto-arteritis (Takayasu's disease) in children." British Journal of Radiology 64, no. 764 (1991): 690–98. http://dx.doi.org/10.1259/0007-1285-64-764-690.

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Scott, Christiaan, Mignon McCulloch, and Peter Nourse. "Takayasus Arteritis in Children: A Developing World Perspective." Annals of Paediatric Rheumatology 2, no. 4 (2013): 134. http://dx.doi.org/10.5455/apr.120320130832.

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20

Jain, S., N. Sharma, S. Singh, H. K. Bali, L. Kumar, and B. K. Sharma. "Takayasu Arteritis in children and young Indians." International Journal of Cardiology 75 (August 2000): S153—S157. http://dx.doi.org/10.1016/s0167-5273(00)00180-7.

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Ladapo, Taiwo Augustina, Priya Gajjar, Mignon McCulloch, Christiaanah Scott, Alp Numanoglu, and Peter Nourse. "Impact of revascularization on hypertension in children with Takayasu’s arteritis-induced renal artery stenosis: a 21-year review." Pediatric Nephrology 30, no. 8 (2015): 1289–95. http://dx.doi.org/10.1007/s00467-015-3049-y.

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22

Dzhus, Marta, and Halyna Mostbauer. "Coronary artery lesions in Takayasu arteritis." Rheumatology 61, no. 6 (2024): 460–72. http://dx.doi.org/10.5114/reum/176483.

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IntroductionTakayasu arteritis (TAK) is a granulomatous inflammation of vessels of large diameter, mainly affecting the aorta and its proximal branches, which is more common in young women. The incidence of coronary artery disease in TAK is unknown and not sufficiently studied.Material and MethodsA literature review was performed for the period 2003 to 2023 using a search of the PubMed and Scopus scientific databases. We used the following key words to search the academic journal data-bases: “Takayasu arteritis”, “coronary angiography”, “myocardial revascularization”, “coronary artery disease”

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23

Wang, C., H. Song, Z. Yu, and M. Quan. "AB1009 THE EFFICACY OF TOCILIZUMAB ON THE TREATMENT OF TAKAYASU ARTERITIS IN CHINESE CHILDREN." Annals of the Rheumatic Diseases 79, Suppl 1 (2020): 1798.2–1798. http://dx.doi.org/10.1136/annrheumdis-2020-eular.5778.

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Background:Takayasu arteritis (TA) is the most prevalent large-vessel vasculitis in children. Patients with TA have a high mobidity and mortality.It remains a therapeutic challenge because corticosteroids monotherapy can rarely cure TAK and the relapse rate is high during GC tapering.Objectives:The aim of this study is to investigate the efficacy and safety of tocilizumab (TCZ)in Chinese children with Takayasu arteritis(TAK).Methods:We retrospectively studied 6 TAK children treated with TCZ in our hospital from July 2017 to October 2018. The demographic and clinical data, laboratory examinatio

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24

Oh, Ah Young, Jong Hwan Lee, Beyoung Soo Kim, et al. "Anesthetic Management of Children with Takayasu's Arteritis: Case reports." Korean Journal of Anesthesiology 43, no. 3 (2002): 384. http://dx.doi.org/10.4097/kjae.2002.43.3.384.

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Maytbasova, R., and P. Ishuova. "AB0566 Outcomes of Takayasu's Arteritis in Children and Adolescents." Annals of the Rheumatic Diseases 75, Suppl 2 (2016): 1098.2–1098. http://dx.doi.org/10.1136/annrheumdis-2016-eular.5830.

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Di Santo, Marisa, Erica V. Stelmaszewski, and Alejandra Villa. "Takayasu arteritis in paediatrics." Cardiology in the Young 28, no. 3 (2017): 354–61. http://dx.doi.org/10.1017/s1047951117001998.

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AbstractTakayasu arteritis is an idiopathic chronic granulomatous panarteritis predominantly affecting the aorta and its main branches. Although idiopathic, genetic contribution to disease susceptibility is being increasingly recognised. Rare in children, Takayasu arteritis is a worldwide disease with significant morbidity and mortality. Its diagnosis is a challenge and requires awareness of the condition as clinical features at presentation are non-specific and assessing disease activity is difficult. In the inflammatory stage, treatment is essential to prevent the insidious course and vascul

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Tireli, Emin, A. Kubilay Korkut, Eylül Kafali, and Murat Basaran. "Successful Repair of Ascending Aortic Aneurysm Due to Takayasu's Arteritis." Asian Cardiovascular and Thoracic Annals 10, no. 2 (2002): 184–85. http://dx.doi.org/10.1177/021849230201000225.

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A 2-year-old girl with Takayasu's arteritis and an ascending aortic aneurysm underwent successful graft replacement. Although aneurysms of the great vessels are rarely encountered, this disease should be considered in the differential diagnosis of ascending aortic aneurysms in children.

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Aly, Doaa, and Natalie Jayaram. "TAKAYASU'S ARTERITIS: A RARE CAUSE OF HEART FAILURE IN CHILDREN." Journal of the American College of Cardiology 71, no. 11 (2018): A2421. http://dx.doi.org/10.1016/s0735-1097(18)32962-0.

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Onan, Sertac Hanedan, Ali Baykan, Sadettin Sezer, et al. "PP-141 TAKAYASU ARTERITIS IN TWO CHILDREN; CASE REPORT." International Journal of Cardiology 140 (April 2010): S80—S81. http://dx.doi.org/10.1016/s0167-5273(10)70286-2.

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Aeschlimann, Florence A., Francesca Raimondi, Tim Leiner, Giovanni Donato Aquaro, David Saadoun, and Heynric B. Grotenhuis. "Overview of Imaging in Adult- and Childhood-onset Takayasu Arteritis." Journal of Rheumatology 49, no. 4 (2021): 346–57. http://dx.doi.org/10.3899/jrheum.210368.

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Takayasu arteritis is an idiopathic large-vessel vasculitis that affects young adults and children and can lead to ischemia and end-organ damage. Vascular imaging is crucial for diagnosis, assessment of disease extent, and management of the disease. Here we critically review evidence for the clinical use of the different imaging modalities: conventional angiography, magnetic resonance imaging, computed tomography, Doppler ultrasound, and 18fluorodeoxyglucose positron emission tomography. We thereby focus on their clinical applicability, challenges, and specific use in children.

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Hahn, Deirdré, Peter D. Thomson, Udai Kala, Peter G. Beale, and Solomon E. Levin. "A review of Takayasu's arteritis in children in Gauteng, South Africa." Pediatric Nephrology 12, no. 8 (1998): 668–75. http://dx.doi.org/10.1007/s004670050526.

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Hong, Chang Yee, Yong Soo Yun, Jung Yun Choi, et al. "Takayasu arteritis in Korean children: Clinical report of seventy cases." Heart and Vessels 7, S1 (1992): 91–96. http://dx.doi.org/10.1007/bf01744551.

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Tullus, Kjell. "Management of the renovascular disease in children with Takayasu arteritis." Pediatric Nephrology 30, no. 8 (2015): 1213–16. http://dx.doi.org/10.1007/s00467-015-3093-7.

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Rao, A. R. Santosh, Vinay Jahagirdar, and Kaanthi Rama. "Catching Takayasu Early: Diagnosing the “Pulseless” Disease in a Child with Palpable Pulses." Case Reports in Pediatrics 2021 (May 27, 2021): 1–5. http://dx.doi.org/10.1155/2021/8885944.

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Takayasu arteritis is a systemic vasculitis of large vessels that mainly involves the aorta and its branches. It normally presents in the third decade of life and is rarely seen in children. We report a case of childhood Takayasu arteritis, in a 12-year-old girl, who presented with abdominal pain and hypertension. Although all her peripheral pulses were palpable, there was a discrepancy between her upper and lower limbs’ blood pressure. CT angiography revealed stenosis of the abdominal aorta, at the origin of the celiac artery and right renal artery. She was started on steroids and an antihype

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Bikouli, Efstathia Danai C., Andriani Vazeou, Maria Xatzipsalti, Georgios Servos, Dimitrios Delis, and Despoina N. Maritsi. "Blau Syndrome Complicated by Atypical Type IIa Takayasu Arteritis." Journal of Child Science 11, no. 01 (2021): e313-e316. http://dx.doi.org/10.1055/s-0041-1740463.

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AbstractBlau syndrome (BS) is a rare, autosomal dominant monogenic autoinflammatory disease, usually presenting as a triad of symptoms (granulomatous dermatitis, uveitis, and nonerosive arthritis) and caused by gain-of-function mutations in the nucleotide oligomerization domain 2 (NOD2) gene. However, very few reports in children of copresence of BS with large vessel vasculitis exist. We hereby describe a case of BS associated with clinical features of Takayasu arteritis. An 8.5-year-old boy presented with hypertension, cardiac insufficiency, arthritis, and ocular disease. Among other investig

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Peremans, Lieselot, Marinka Twilt, Susanne M. Benseler, et al. "Real-World Biomarkers for Pediatric Takayasu Arteritis." International Journal of Molecular Sciences 25, no. 13 (2024): 7345. http://dx.doi.org/10.3390/ijms25137345.

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Childhood-onset Takayasu arteritis (TA) is a rare, heterogeneous disease with limited diagnostic markers. Our objective was to identify and classify all candidates for biomarkers of TA diagnosis in children reported in the literature. A systematic literature review (PRISMA) of MEDLINE, EMBASE, Wiley Cochrane Library, ClinicalTrias.gov, and WHO ICTRP for articles related to TA in the pediatric age group between January 2000 and August 2023 was performed. Data on demographics, clinical features, laboratory measurements, diagnostic imaging, and genetic analysis were extracted. We identified 2026

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Podzolkova, V. A., G. A. Lyskina, Yu O. Kostina, and V. A. Seraya. "EXPERIENCE OF USING TOCILIZUMAB IN THERAPY OF TAKAYASU ARTERITIS IN CHILDREN." Pediatria. Journal named after G.N. Speransky 100, no. 5 (2021): 145–51. http://dx.doi.org/10.24110/0031-403x-2021-100-5-145-151.

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The prognosis of Takayasu arteritis (TA) depends on timely and adequate therapy, but in about half of patients, the disease is refractory to standard therapy or recurs against the background of a decrease in the dose of glucocorticoids (GCs). The use of biological disease-modifying antirheumatic drugs (bDMARDs) in the treatment of TA looks promising, however, the experience of their use in TA in children is presented by isolated observations. Objective of the study: to evaluate the efficacy and safety of tocilizumab (TCZ) in the treatment of refractory and recurrent forms of TA in children. Ma

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Marks, Stephen D., and Kjell Tullus. "Do classification criteria of Takayasu arteritis misdiagnose children with fibromuscular dysplasia?" Pediatric Nephrology 25, no. 5 (2010): 989–90. http://dx.doi.org/10.1007/s00467-009-1419-z.

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Wirawan, Muhammad Taufik, Indah Kartika Murni, Suryono Yudha Patria, Nadya Arafuri, Noormanto Noormanto, and Sasmito Nugroho. "Undetected Takayasu arteritis presenting as severe hypertension in children: a report of two cases." Paediatrica Indonesiana 64, no. 5 (2024): 454–8. http://dx.doi.org/10.14238/pi64.5.2024.454-8.

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Takayasu arteritis (TA) is a rare chronic granulomatous vasculitis mainly affecting the aorta and its main branches. Clinical presentations of TA are non-specific, especially in the initial phase, which likely contributes to delayed diagnosis besides the rarity of the disorder. Childhood-onset of TA is associated with significant morbidity and mortality. This case report aimed to present two rare cases of acute symptomatic severe hypertension in children due to TA.

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Goel, Ruchika, T. Sathish Kumar, Debashish Danda, et al. "Childhood-onset Takayasu Arteritis — Experience from a Tertiary Care Center in South India." Journal of Rheumatology 41, no. 6 (2014): 1183–89. http://dx.doi.org/10.3899/jrheum.131117.

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Objective.To study the clinical profile and outcome of Asian Indian children with childhood-onset Takayasu arteritis (c-TA).Methods.Records were studied of patients with c-TA onset prior to age 16. Disease Extent Index-Takayasu (DEI.TAK), Indian Takayasu Arteritis Score 2010, and Takayasu Arteritis Damage Score (TADS) were calculated retrospectively from electronic records. Cumulative incidence of sustained remission was estimated using the Kaplan-Meier curve.Results.There were 40 patients with c-TA, with median age of onset of 12.5 years (range 1–16) and median diagnostic delay of 11.3 months

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Fieldston, Evan, Daniel Albert, and Terri Finkel. "Hypertension and Elevated ESR as Diagnostic Features of Takayasu Arteritis in Children." JCR: Journal of Clinical Rheumatology 9, no. 3 (2003): 156–63. http://dx.doi.org/10.1097/01.rhu.0000073436.33243.2c.

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Kostina, Y., and G. Lyskina. "FRI0282 Experience of Biological Agents Treatment of Refractory Takayasu Arteritis in Children." Annals of the Rheumatic Diseases 74, Suppl 2 (2015): 527.1–527. http://dx.doi.org/10.1136/annrheumdis-2015-eular.3411.

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Goel, R., D. Danda, S. Kumar, and G. Joseph. "A single centre experience of 40 children with Takayasu arteritis from India." La Presse Médicale 42, no. 4 (2013): 728–29. http://dx.doi.org/10.1016/j.lpm.2013.02.182.

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Tullus, Kjell, and Derek J. Roebuck. "Renovascular hypertension in small children—is it Takayasu arteritis or fibromuscular dysplasia?" Journal of the American Society of Hypertension 12, no. 7 (2018): 506–8. http://dx.doi.org/10.1016/j.jash.2018.04.011.

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Anguita, Rodrigo, Cristobal Nazar, Rudolf Kobus, Alejandro Salinas, and Maria Astete. "Bilateral ocular ischemic syndrome as a manifestation of Takayasu arteritis in children." Canadian Journal of Ophthalmology 54, no. 3 (2019): e105-e108. http://dx.doi.org/10.1016/j.jcjo.2018.08.018.

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Zhang, Wenting, Ziqi Xu, Yamin Shu, Sainan Shu, and Qilin Zhang. "Adverse Event Profiles of Adalimumab in Children: A Disproportionality Analysis." Pharmaceuticals 17, no. 8 (2024): 1028. http://dx.doi.org/10.3390/ph17081028.

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Background: Adalimumab has been approved by the U.S. Food and Drug Administration (FDA) for the treatment of adult rheumatoid arthritis (RA), and subsequently approved for pediatric treatment of various autoimmune diseases in children of different ages. Due to genetic differences between children and adults in terms of physiology and immunity, there is a need to explore the safety of adalimumab in children in the real world. The aim of this study is to identify potential adverse event (AE) signals associated with the use of adalimumab in pediatric patients (<18 years old) using data from th

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Dr., Soumyashree Bahalia, Samar Pratim Nayak Dr., Sunil Kumar Agarwalla Dr., et al. "A Rare Presentation of Dilated Cardiomyopathy Along with Takayasu Arteritis in a Preschool Child." INTERNATIONAL JOURNAL OF MEDICAL SCIENCE AND CLINICAL RESEARCH STUDIES 03, no. 08 (2023): 1529–31. https://doi.org/10.5281/zenodo.8217228.

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Dilated cardiomyopathy is the most common form of cardiomyopathy in children, is the cause of significant morbidity and mortality. Although the most common etiology of DCM remains idiopathic, it is estimated that upto 50% of cases are genetic. The pathogenesis of ventricular dilation and altered contractility seen in DCM varies depending on the underlying etiology; systolic dysfunction and myocyte injury are common.   Takayasu arteritis also known as “pulseless disease”, is a chronic large vessel vasculitis of unknown etiology and predominantly involves the aorta and its major

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Aluquin, V. P. R. "Magnetic resonance imaging in the diagnosis and follow up of Takayasu's arteritis in children." Annals of the Rheumatic Diseases 61, no. 6 (2002): 526–29. http://dx.doi.org/10.1136/ard.61.6.526.

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Koneti, Nageswara Rao, Nipun Mahajan, Shweta Bakhru, Sudeep Verma, and Pallavi Kathare. "Emergency renal artery stenting in acute anuric renal failure in children with Takayasu's arteritis." Indian Heart Journal 65, no. 5 (2013): 600–602. http://dx.doi.org/10.1016/j.ihj.2013.08.018.

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Zhu, Wei-Hua, Lai-Gen Shen, and Henning Neubauer. "Clinical characteristics, interdisciplinary treatment and follow-up of 14 children with Takayasu arteritis." World Journal of Pediatrics 6, no. 4 (2010): 342–47. http://dx.doi.org/10.1007/s12519-010-0234-8.

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