Mathews Journal of Case Reports Hydranencephaly

نویسندگان

  • Mohammad Nawaz Nasery
  • Farhad Farzam
  • Hidayatullah Hamidi
  • Jamshid Sadiqi
  • Ahmad Reshad Faizi
  • Fazel Rahman Faizi
  • Marzia Mohammadi
  • Ali Abad
چکیده

Mathews Journal of Case Reports Hydranencephaly Mohammad Nawaz Nasery1, Farhad Farzam1, Hidayatullah Hamidi2, Jamshid Sadiqi2, Ahmad Reshad Faizi2, Fazel Rahman Faizi2, Marzia Mohammadi2 1Radiology department, Ali Abad Teaching Hospital, Kabul, Afghanistan. 2Radiology department, French Medical Institute for Children (FMIC), Kabul, Afghanistan. Corresponding Author: Mohammad Nawaz Nasery, Ali Abad Teaching Hospital Kabul, Afghanistan, Tel: +93 20 250 0522; Email: [email protected]

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منابع مشابه

The histopathology of a case of hydranencephaly in a 30 week old human fetus.

Kuhlenbeck and Globus ('36) described a case of Arhinencephaly with eversion of the forebrain of an infant four days after birth. Kuhlenbeck, Hafkesbring and Ross ('59) made some observations on a living decorticate hydranencephalic child. Their findings indicated a growth disturbance of the forebrain. Kuhlenbeck, Maher, Ross and Eastwood ('57) made some comments, with anatomical and clinical o...

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Endoscopic Coagulation of Choroid Plexus in Hydranencephaly

Hydranencephaly is a rare congenital disease defined as an absence of cerebral hemispheres with an intact thalamus, brain stem, and cerebellum. Generally, patients with hydranencephaly require cerebro-spinal fluid diversion due to progressive hydrocephalus. An excellent view of the choroid plexus and advancement of the neurosurgical endoscope were possible, leading to easy coagulation of the ch...

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Hydranencephaly: a rare cause of delayed developmental milestones.

To cite: Malik AM, Ahmad M, Khan A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-009589 DESCRIPTION A 2-year-old female child presented with a history of delayed developmental milestones. According to her mother, the child was born out of a normal vaginal delivery and was apparently well after birth. However, by 6 months of age, the mother noticed ...

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A rare variation of hydranencephaly: case report

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 prese...

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Hydranencephaly: Considering Prolonged Survival and Treatment by Endoscopic Choroid Plexus Coagulation.

Arachnoid collapse is a previously unreported complication of endoscopic choroid plexus coagulation (ECPC) treatment of hydranencephaly and is demonstrated in this case report. The variable anatomy found in hydranencephaly supports the use of ECPC as the preferred treatment option. However, the same anatomical anomalies predispose the procedure to this unique complication. A brief literature re...

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تاریخ انتشار 2017