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Journal articles on the topic 'Hydranencephaly'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Malheiros, José Augusto, Felipe Padovani Trivelato, Marcelo Magaldi Oliveira, Sebastião Gusmão, David Douglas Cochrane, and Paul Steinbok. "Endoscopic Choroid Plexus Cauterization Versus Ventriculoperitoneal Shunt for Hydranencephaly and Near Hydranencephaly." Neurosurgery 66, no. 3 (2010): 459–64. http://dx.doi.org/10.1227/01.neu.0000365264.99133.ca.

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Abstract OBJECTIVE To prospectively evaluate the results of endoscopic choroid plexus cauterization (ECPC) and ventriculoperitoneal shunts (VPSs) in infants with hydranencephaly or near hydranencephaly. METHODS We prospectively collected clinical data from all untreated hydranencephalic and near hydranencephalic children from October 2006 to March 2008. All patients treated were randomly divided into 2 groups, ECPC or VPS, and submitted to either endoscopic choroid plexus cauterization or ventriculoperitoneal shunt placement. RESULTS Seventeen patients were entered into the study. ECPC was com

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2

Gentry, Millicent, and Mary Connell. "Hydranencephaly." Ultrasound Quarterly 29, no. 3 (2013): 267–68. http://dx.doi.org/10.1097/ruq.0b013e3182a33715.

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Pinar, Halit. "Hydranencephaly." Pathology Case Reviews 16, no. 5 (2011): 186–88. http://dx.doi.org/10.1097/pcr.0b013e318229862e.

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4

Sharma, Akshay, Deeksha Sharma, and Pranav Pandoh. "HYDRANCEPHALY : RARE ENTITY WITH INCIDENCE LESS THAN 1 IN 10000 LIVE BIRTHS." International Journal of Advanced Research 9, no. 02 (2021): 678–80. http://dx.doi.org/10.21474/ijar01/12497.

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Hydranencephaly is a rare entity with incidence of 1 in 10000 live births and is characterized by near total absence of cerebral cortex and basal ganglia which are replaced by cerebrospinal fluid. Various aetiologies of hydranencephaly have been suggested which include: Infarction, leukomalacia, diffuse hypoxic-ischemic brain necrosis, intrauterine infections leading to necrotizing vasculitis. Ultrasonography, Computed Tomography and Magnetic Resonance Imaging can easily detect and diagnose hydranencephaly. We present a case of 2-month-old term infant diagnosed with hydranencephaly on computed

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5

Baidi, H., M. Sellouti, A. Ayad, and R. Abilkassem. "Monochorionic Twin Pregnancy with Hydranencephaly and Co-Twin Death: A Case Report." Asian Journal of Pediatric Research 14, no. 8 (2024): 18–24. http://dx.doi.org/10.9734/ajpr/2024/v14i8377.

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Background: Hydranencephaly is a rare congenital brain malformation with an incidence estimated to be between 1 in 10 000 and 1 in 5 000 pregnancies. It is characterized by the absence of development of the cerebral hemispheres, which are replaced by cerebrospinal fluid. The diagnosis of hydranencephaly can be made from 15 weeks of amenorrhea via obstetric ultrasound, with antenatal nuclear MRI being the definitive test to establish the diagnosis. The condition results from an anomaly in embryogenesis after the formation of the neural plate, though the exact pathophysiology of hydranencephaly

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6

Andreeva, E. Yu, D. S. Bokieva, and M. M. Bulanova. "Prenatal diagnosis of hydranencephaly: a clinical case." Ultrasound & Functional Diagnostics, no. 2 (June 21, 2024): 63–71. http://dx.doi.org/10.24835/1607-0771-269.

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Hydranencephaly is a rare abnormality of the central nervous system (CNS) of the fetus, in which the cerebral hemispheres are absent and replaced with cerebrospinal fluid, while the structures of the posterior fossa, thalami and falx cerebri remains normal. The ischemic, hemorrhagic complications, infection of the fetus, the toxic effects of carbon monoxide, butane and genetic abnormalities are potential causes of a hydranencephaly development. The article presents the modern data on the possible causes of the hydranencephaly development, and clinical case of prenatal ultrasound diagnosis of h

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Dehneh, Younes, Mohammed Khoulali, Noureddine Oulali, and Faycel Moufid. "Hydranencephaly Associated with Bilateral Megalocornea and Bilateral Cleft Lip in an Infant of Mother with Gestational Diabetes Mellitus." Indian Pediatrics Case Reports 4, no. 1 (2024): 48–50. http://dx.doi.org/10.4103/ipcares.ipcares_186_23.

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Abstract Background: Hydranencephaly is a rare congenital disorder of the central nervous system, in which the cerebrum is replaced by a membranous sac of cerebrospinal fluid. Clinical Description: A 2-month-old baby girl presented with abnormal body movements. She was born to a mother with gestational diabetes and had been diagnosed with hydrocephalus antenatally. The baby had features of facial dysmorphism such as bilateral megalocornea, bilateral cleft lip, and cleft palate. A magnetic resonance imaging (MRI) brain revealed the absence of cerebral hemispheres with remnants of parenchyma in

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8

M. Al-Abdallat, Imad, Ibrahim H. Alhabash, Asma M. Alshaeb, and Hasan A. Abder-Rahman. "Was the Hydranencephaly Defense Valid for the Death of a Child?: A Case Report." Arab Journal of Forensic Sciences and Forensic Medicine 3, no. 2 (2021): 331–35. http://dx.doi.org/10.26735/rbjb7151.

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Hydranencephaly is a central nervous system disorder at birth in which brain's cerebral hemispheres are absent and replaced by sacks filled with CSF. The prevalence of hydranencephaly is less than 1 in 10,000 births, with 0.2 percent of children autopsies showing the condition.

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9

Oriaifo, Bosede Belinda, Stephen Ohikhuemei Izevbekhai, Chukwudi Nnaedozie Ahunanya, Pamela Faith Isioma Irabor, and Evelyn Oshodin. "Ultrasound Diagnosed Fetal Hydranencephaly in the Prenatal Period." Journal of Radiation Medicine in the Tropics 5, no. 1 (2024): 31–33. http://dx.doi.org/10.4103/jrmt.jrmt_5_24.

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Abstract Hydranencephaly is a rare congenital encephalopathy characterized by a near complete absence of the cerebral cortical mantle and basal ganglia, with consequent replacement by cerebrospinal fluid (CSF). Although hydranencephaly is an extremely rare congenital entity with an incidence <1/10,000 live births, there are no known gender or racial predilections. However, polyhydramnios is a recognized association. Brain infarction from bilateral internal carotid artery occlusion, fetal hypoxia, leukomalacia, and congenital infections have all been implicated as possible etiologies for thi

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10

Ramesh, Vengalathur Ganesan. "Hydranencephaly Vs Hydrocephalus." Neurosurgery 67, no. 5 (2010): E1472. http://dx.doi.org/10.1227/neu.0b013e3181f36010.

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11

Kurtz, Alfred B., and Pamela T. Johnson. "Case 7: Hydranencephaly." Radiology 210, no. 2 (1999): 419–22. http://dx.doi.org/10.1148/radiology.210.2.r99fe50419.

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12

Tsai, Jeng-Dau, Huang-Tsung Kuo, and I.-Ching Chou. "Hydranencephaly in Neonates." Pediatrics & Neonatology 49, no. 4 (2008): 154–57. http://dx.doi.org/10.1016/s1875-9572(08)60032-7.

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13

Aoki, Nobuhiko. "Hydrocephalus or hydranencephaly." Surgical Neurology 25, no. 6 (1986): 600. http://dx.doi.org/10.1016/0090-3019(86)90191-6.

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14

Vishnoi, Dakshata, Ekansh Rathoria, Gaurav Dutta, Shaik Aalam, Nalin Shukla, and Jitendra Kumar Singh. "Hydranencephaly: a rare case report on enlarging head in an infant." International Journal of Scientific Reports 11, no. 4 (2025): 171–75. https://doi.org/10.18203/issn.2454-2156.intjscirep20250750.

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Hydranencephaly is an uncommon congenital disorder in which the cerebral hemispheres are absent and replaced by cerebrospinal fluid. In this article, we describe an uncommon case of hydranencephaly in a 3-month-old male child with complaints of progressively increasing head size over the last 1 month and inability to control his neck. The child was diagnosed as a case of Hydranencephaly by cranial ultrasonography (USG) and further confirmed by computed tomography (CT) and magnetic resonance imaging (MRI) which revealed a complete absence of the cerebral hemisphere with intact falx, brain paren

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15

International, Journal of Medical Science and Innovative Research (IJMSIR). "Radiological Imaging in Hydranencephaly: A Case Report." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 6 (2024): 73–76. https://doi.org/10.5281/zenodo.15449515.

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<strong>Abstract</strong> Hydranencephaly is a rare congenital anomaly characterized by the near-complete absence of the cerebral hemispheres with preservation of the brainstem and basal ganglia. Radiological imaging plays a crucial role in the antenatal and postnatal diagnosis, management, and prognostication of this condition. This abstract provides a comprehensive review of the radiological findings in hydranencephaly. Prenatal ultrasound typically reveals a lack of cerebral tissue with the presence of fluid-filled cranial vaults. Magnetic resonance imaging (MRI) further delineates the exte

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16

Wijerathne, Buddhika TB, Geetha K. Rathnayake, and Sisira K. Ranaraja. "A rare variation of hydranencephaly: case report." F1000Research 1 (January 30, 2013): 22. http://dx.doi.org/10.12688/f1000research.1-22.v2.

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Hydranencephaly is a rare congenital abnormality characterized by the absence and replacement of the cerebral hemispheres with cerebrospinal fluid. Here, we present an ultrasonographic diagnosis of a case of a rare variant of fetal hydranencephaly at 38 weeks of gestation. Obstetric sonography revealed the absence of the cerebral cortex, thalami and basal ganglia with a disrupted falx and preserved posterior fossa structures. This is the first reported case of hydranencephaly with the absence of the thalami and basal ganglia, which was diagnosed prenatally. The diagnosis was confirmed with pos

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Wijerathne, Buddhika TB, Geetha K. Rathnayake, and Sisira K. Ranaraja. "A rare variation of hydranencephaly: case report." F1000Research 1 (January 30, 2014): 22. http://dx.doi.org/10.12688/f1000research.1-22.v3.

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Hydranencephaly is a rare congenital abnormality characterized by the absence and replacement of the cerebral hemispheres with cerebrospinal fluid. Here, we present an ultrasonographic diagnosis of a case of a rare variant of fetal hydranencephaly at 38 weeks of gestation. Obstetric sonography revealed the absence of the cerebral cortex, thalami and basal ganglia with a disrupted falx and preserved posterior fossa structures. This is the first reported case of hydranencephaly with the absence of the thalami and basal ganglia, which was diagnosed prenatally. The diagnosis was confirmed with pos

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18

Avidan, O., A. Craig, and K. Deerwester. "An Infant with Neonatal Abstinence Syndrome in the Setting of Hydranencephaly." Journal of Pediatric Neurology 17, no. 01 (2017): 038–40. http://dx.doi.org/10.1055/s-0037-1608948.

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AbstractAn infant of 37 weeks' gestation was born with signs and symptoms of neonatal abstinence syndrome (NAS). Upon further investigation, he was found to have congenital hydranencephaly, a condition in which the forebrain is absent. In this case report, we explore the mechanisms of NAS and hydranencephaly, and why an infant without a forebrain can still experience NAS symptoms.

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19

Chaja, W., A. Garmane, I. Daha, B. Zouita, D. Basraoui, and H. Jalal. "Hydranencephaly: A Case Report." Scholars Journal of Medical Case Reports 11, no. 10 (2023): 1829–31. http://dx.doi.org/10.36347/sjmcr.2023.v11i10.027.

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Hydranencephaly is a congenital neurodevelopmental anomaly in which there is an absence of the cerebral hemispheres and intact infratentorial structures. Diagnosis can be made prenatally or postnatally using ultrasound, CT, or MRI. Imaging findings include the presence of primitive brain structures, variable presence of the falx cerebri, and total or near-total absence of the cerebral hemispheres. We reported a case of newborn hydranencephaly in 1 day old neonate with macrocephaly.

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20

Sen, Kuntal, Shagun Kaur, David W. Stockton, Mary Nyhuis, and Jacquelyn Roberson. "Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy." American Journal of Perinatology Reports 11, no. 01 (2021): e26-e28. http://dx.doi.org/10.1055/s-0040-1722728.

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Abstract Case Report A 32-year-old female with a history of three prior pregnancy losses presented for genetic testing following an ultrasonography diagnosis of fetal hydranencephaly. Baby was born via C-section and was noted to have a head circumference of 48 cm, in addition to ocular and cardiac anomalies and dysmorphic features. Whole genome sequencing revealed a homozygous variant in LAMB1 gene. Discussion The pathobiogenesis of hydranencephaly is incompletely understood and is attributed to vascular, infectious, or genetic etiology. Herein we present LAMB1 as a monogenic cause of fetal hy

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21

Wijerathne, Buddhika TB, Geetha K. Rathnayake, and Sisira K. Ranaraja. "A rare variation of hydranencephaly: case report." F1000Research 1 (October 3, 2012): 22. http://dx.doi.org/10.12688/f1000research.1-22.v1.

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Hydranencephaly is a rare severe abnormality characterized by replacement of cerebral hemisphere with fluid covered by leptomeninges such that absent cerebral cortex. We present the Ultrasonographic diagnosis of a case of fetal Hydranencephaly at 38 weeks of gestation. Sonography revealed the absence of cerebral cortex, thalami and basal ganglia with disrupted falx and preserved posterior fossa structures. This was the first reported case of Hydranencephaly with absence thalami and basal ganglia along with midbrain. Confirmation of diagnosis was made with postnatal computed tomography. Even th

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22

Ro, H. J., Y. I. Lee, S. Y. Lee, et al. "CT findings of hydranencephaly." Journal of the Korean Radiological Society 23, no. 5 (1987): 730. http://dx.doi.org/10.3348/jkrs.1987.23.5.730.

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23

Sepulveda, Waldo, Hernan Cortes-Yepes, Amy E. Wong, Victor Dezerega, Edgardo Corral, and Gustavo Malinger. "Prenatal Sonography in Hydranencephaly." Journal of Ultrasound in Medicine 31, no. 5 (2012): 799–804. http://dx.doi.org/10.7863/jum.2012.31.5.799.

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24

Herman, David C., George B. Bartley, and John D. Bullock. "Ophthalmic Findings of Hydranencephaly." Journal of Pediatric Ophthalmology & Strabismus 25, no. 3 (1988): 106–11. http://dx.doi.org/10.3928/0191-3913-19880501-03.

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25

Lorber, John. "Hydranencephaly with Normal Development." Developmental Medicine & Child Neurology 7, no. 6 (2008): 628–33. http://dx.doi.org/10.1111/j.1469-8749.1965.tb07839.x.

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26

Baiker, K., N. Saunders, B. A. Summers, R. J. Piercy, and K. Smith. "Hydranencephaly in a foal." Equine Veterinary Education 22, no. 12 (2010): 593–98. http://dx.doi.org/10.1111/j.2042-3292.2010.00123.x.

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27

NORMAN, A. M., and D. DONNAI. "Hypoplastic thumbs and hydranencephaly." Clinical Dysmorphology 1, no. 2 (1992): 121. http://dx.doi.org/10.1097/00019605-199204000-00009.

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28

Tayama, Masanobu, Toshiaki Hashimoto, Kenji Mori, et al. "Electrophysiological study on hydranencephaly." Brain and Development 14, no. 3 (1992): 185–87. http://dx.doi.org/10.1016/s0387-7604(12)80263-4.

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29

Merker, Bjorn. "Life expectancy in hydranencephaly." Clinical Neurology and Neurosurgery 110, no. 3 (2008): 213–14. http://dx.doi.org/10.1016/j.clineuro.2007.11.011.

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30

Shitsama, Sylvia, Nunthasiri Wittayanakorn, Humphrey Okechi, and A. Leland Albright. "Choroid plexus coagulation in infants with extreme hydrocephalus or hydranencephaly." Journal of Neurosurgery: Pediatrics 14, no. 1 (2014): 55–57. http://dx.doi.org/10.3171/2014.3.peds13488.

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Object Severe hydrocephalus and hydranencephaly are common congenital conditions in Kenya. In patients with these conditions, ventriculoperitoneal (VP) shunts are associated with appreciable complications and endoscopic third ventriculostomies (ETVs) have limited success. Endoscopic choroid plexus coagulation (CPC) to diminish CSF production is a potential treatment option. The purpose of this study was to evaluate the effect of CPC without ETV in infants with severe hydrocephalus or hydranencephaly. Methods Medical records of infants with severe congenital hydrocephalus or hydranencephaly who

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31

Zhang, Hui, Patrick Manda, Tianze Sun, Blessed Kondowe, Dong Wang, and Jin Shang. "Hydranencephaly: exploring the role of CT features in the diagnosis of 22 cases." Malawi Medical Journal 36, no. 5 (2025): 313–17. https://doi.org/10.4314/mmj.v36i5.4.

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ObjectiveTo delve into the clinical and CT imaging manifestations of hydranencephaly, a rare congenital post-neurulation disorder occurring during the second trimester, characterized by the destruction of cerebral hemispheres and cranial cavity filled with cerebrospinal fluid (CSF). This research aims to enhance our understanding of hydranencephaly and establish a standard for its imaging diagnosis.Methods A retrospective analysis was conducted using the brain CT images and clinical data of 26 pediatric patients diagnosed with hydranencephaly.Results At birth, the primitive reflexes were gener

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32

Dewiyanti, Lilia, Andrew Robert Diyo, Jonathan Edbert Afandy, Jennefer ., and Cipta Pramana. "Case Report: Hydranencephaly in a female newborn with congenital cytomegalovirus infection." F1000Research 11 (June 13, 2022): 199. http://dx.doi.org/10.12688/f1000research.108934.2.

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Background: Hydranencephaly is a congenital abnormality of the central nervous system characterized by massive hemispheric necrosis and ventricular dilatation with most of the cerebral hemispheres being replaced by membranous sacs filled with cerebrospinal fluid (CSF). Cytomegalovirus (CMV) infection can be one of the causes of hydranencephaly. The choice of therapy for hydranencephaly is a challenge because of poor prognosis, but now neural stem cell (NSC) transplantation may give new hope. Case report: We report a case of a female newborn born at term by cesarean section from a gravida 5, pa

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Dewiyanti, Lilia, Andrew Robert Diyo, Jonathan Edbert Afandy, Jennefer ., and Cipta Pramana. "Case Report: Hydranencephaly in a female newborn with congenital cytomegalovirus infection." F1000Research 11 (February 16, 2022): 199. http://dx.doi.org/10.12688/f1000research.108934.1.

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Background: Hydranencephaly is a congenital abnormality of the central nervous system characterized by massive hemispheric necrosis and ventricular dilatation with most of the cerebral hemispheres being replaced by membranous sacs filled with cerebrospinal fluid (CSF). Cytomegalovirus (CMV) infection can be one of the causes of hydranencephaly. The choice of therapy for hydranencephaly is a challenge because of poor prognosis, but now neural stem cell (NSC) transplantation may give new hope. Case report: We report a case of a female newborn born at term by cesarean section from a gravida 5, pa

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34

Huff, Nicholas, and Sunil Naik. "Hydranencephaly in Monochorionic-Diamniotic Twins." Pediatric Neurology 67 (February 2017): 107–8. http://dx.doi.org/10.1016/j.pediatrneurol.2016.08.002.

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35

Sener, R. Nuri. "Congenital cytomegalovirus infection and hydranencephaly." Radiography 2, no. 3 (1996): 229–32. http://dx.doi.org/10.1016/s1078-8174(96)90055-3.

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36

Gopinathan, Shalini, Simrita Khurana, VP Singh, RK Gupta, and AK Dubey. "Is it Hydranencephaly – A Variant?" Medical Journal Armed Forces India 58, no. 4 (2002): 338–39. http://dx.doi.org/10.1016/s0377-1237(02)80093-4.

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37

Donadono, V., G. Esposito, R. Napolitano, et al. "P17.12: Prenatal diagnosis of hydranencephaly." Ultrasound in Obstetrics & Gynecology 40, S1 (2012): 239. http://dx.doi.org/10.1002/uog.12002.

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38

Lubinsky, Mark S., William Adkins, and Elizabeth G. Kaveggia. "Decreased maternal age with hydranencephaly." American Journal of Medical Genetics 69, no. 3 (1997): 232–34. http://dx.doi.org/10.1002/(sici)1096-8628(19970331)69:3<232::aid-ajmg3>3.0.co;2-n.

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39

Thiong’o, Grace M., Susan S. Ferson, and A. Leland Albright. "Hydranencephaly treatments: retrospective case series and review of the literature." Journal of Neurosurgery: Pediatrics 26, no. 3 (2020): 228–31. http://dx.doi.org/10.3171/2020.3.peds19596.

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OBJECTIVEThe objective of this study was to review treatment options for infants with hydranencephaly and to consider the pros and cons of each treatment modality.METHODSThis paper is a review of hydranencephaly as well as a retrospective analysis evaluating the outcomes of 52 infants with hydranencephaly who were treated at the Kijabe Hospital, Kijabe, Kenya, in one of four ways: ventriculoperitoneal shunt (VPS) insertion, endoscopic choroid plexus coagulation (CPC), open choroid plexectomy (CPlx), and palliative care. The primary outcome measure was control of head size, with the aim of impr

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40

sultana, Zafar, Anantha kumari, and Habib G. Pathan. "A RARE CASE OF HYDRANENCEPHALY: A CASE REPORT." International Journal of Anatomy and Research 8, no. 3.2 (2020): 7644–48. http://dx.doi.org/10.16965/ijar.2020.152.

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41

Edwards, J. F., C. W. Livingston, S. I. Chung, and E. C. Collisson. "Ovine Arthrogryposis and Central Nervous System Malformations Associated with in utero Cache Valley Virus Infection: Spontaneous Disease." Veterinary Pathology 26, no. 1 (1989): 33–39. http://dx.doi.org/10.1177/030098588902600106.

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Gross appearance and histologic lesions seen in 15 newborn lambs in an outbreak of congenital arthrogryposis with hydrocephalus or hydranencephaly (CAH) in Texas are described. Severe arthrogryposis with skeletal muscle hypoplasia was seen in limbs of affected lambs. Spinal column deformities were also present. Multiple central nervous system (CNS) malformations were present in CAH lambs including micrencephaly, cerebellar hypoplasia, micromelia, hydrocephalus, hydranencephaly, and porencephaly. Histologic lesions consisted primarily of areas of necrosis and loss of the paraventricular neuropi

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42

Kim, J. P., K. S. Cha, K. N. Ryu, S. H. Lee, K. W. Lee, and K. S. Cho. "US and CT findings of hydranencephaly." Journal of the Korean Radiological Society 25, no. 4 (1989): 626. http://dx.doi.org/10.3348/jkrs.1989.25.4.626.

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Chinsky, J. M. "Hydranencephaly: Transillumination May Not Illuminate Diagnosis." NeoReviews 13, no. 4 (2012): e233-e240. http://dx.doi.org/10.1542/neo.13-4-e233.

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Chautakuri, Dr Kishore, Dr Parveen Chandna, and Dr Pramod Setty J. "Scaling New Heights To Diagnose Hydranencephaly." IOSR Journal of Dental and Medical Sciences 15, no. 09 (2016): 04–10. http://dx.doi.org/10.9790/0853-1509030410.

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45

Sedain, Gopal, and Binod Rajbhandari. "Hydranencephaly: Insights into Pathophysiology and Management." Nepal Journal of Neuroscience 17, no. 1 (2020): 5–9. http://dx.doi.org/10.3126/njn.v17i1.28336.

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Hydranencephaly is a rare and severe form of congenital disorder in which there is absence of cerebral cortex which is replaced by fluid. The presentation is in the form of hydrocephalus and developmental delay. There are various reports on possible etiopathogenesis and management. However, the overall prognosis is grim and clinicians especially in low and middle-income countries like Nepal often face a clinical judgement dilemma regarding management options to offer to the patient family. The ethical issue whether to offer cerebrospinal fluid diversion or not is always there. This review is a

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46

Belfar, H. L., J. A. Kuller, L. M. Hill, and S. Kislak. "Evolving fetal hydranencephaly mimicking intracranial neoplasm." Journal of Ultrasound in Medicine 10, no. 4 (1991): 231–33. http://dx.doi.org/10.7863/jum.1991.10.4.231.

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47

Coady, Deborah, Jon Snyder, Ilana Lustig-Gillman, Joseph Suidan, Steven Hori, and Bruce Young. "Hydranencephaly: Prenatal and Neonatal Ultrasonographic Appearance." American Journal of Perinatology 2, no. 03 (1985): 228–30. http://dx.doi.org/10.1055/s-2007-999956.

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48

Rıfkı, HAZIROĞLU. "PATHOLOGICAL FlNDINGS IN CALVES WITH HYDRANENCEPHALY'." Ankara Üniversitesi Veteriner Fakültesi Dergisi 37, no. 2 (1990): 1. http://dx.doi.org/10.1501/vetfak_0000001346.

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49

Pérez-Ferrer, Antonio, Elena Gredilla, Jesús de Vicente, Yolanda Laporta, and Catarina Madeira. "Low bispectral index values in hydranencephaly." European Journal of Anaesthesiology 26, no. 7 (2009): 611–13. http://dx.doi.org/10.1097/eja.0b013e32831bd8e7.

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