- Periventricular Heterotopia: A Case Report
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Lee TN, Park YS, Lee KC, Jung C, Mok JH
- KMID: 1955378
- J Korean Neurosurg Soc.
- 1996 Sep;25(9):1941-1945.
Anomalies of cell migration are due to various kinds of damage(vascular, infectious, teratogenic etc.) which interfere with neuronal migration between the 8th and 24th week of gestation. Periventricular heterotopias are... -
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- A Case of Wolf-Hirschhorn Syndrome with Periventricular Nodular Heterotopia Presenting with Status Epilepticus
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Suh BS, Ko KH, Lee KH, Sung TJ
- KMID: 2130694
- Neonatal Med.
- 2015 Nov;22(4):233-237.
- doi: 10.5385/nm.2015.22.4.233
Wolf-Hirschhorn syndrome is a congenital disorder associated with partial deletion of the short arm of chromosome 4. The majority of patients showed characteristic facial anomalies - so called "Greek-Helmet" appearances... -
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- A case of FLNA gene mutation with respiratory insufficiency and periventricular heterotopia
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Park H, Park MS, Ki CS, Cho J, Lee J, Kim J, Ahn K
- KMID: 2461409
- Allergy Asthma Respir Dis.
- 2019 Jul;7(3):158-164.
- doi: 10.4168/aard.2019.7.3.158
Filamin A is an actin-binding protein and, in humans, is encoded by FLNA gene in the long arm of X chromosome. Filamin A plays a role in the formation of... -
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- Periventricular nodular heterotopia in a child with a mild Mowat–Wilson phenotype caused by a novel missense mutation of ZEB2
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Kim YO, Lee YY, Kim MK, Woo YJ
- KMID: 2470101
- J Genet Med.
- 2019 Dec;16(2):71-75.
- doi: 10.5734/JGM.2019.16.2.71
Periventricular nodular heterotopia (PNH) is a malformation of cortical development in which normal neurons inappropriately cluster in periventricular areas. Patients with Mowat–Wilson syndrome (MWS) typically present with facial gestalt, complex... -
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- A Case of Ependymal Cyst
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An Y, Lee SH, Han DH
- KMID: 1672254
- J Korean Neurosurg Soc.
- 1995 Nov;24(11):1413-1417.
Ependymal cysts are rare entities that have evoked much controversies regarding their pathogenesis. We report a case of an intracerebral ependymal cyst associated with periventricular heterotopia and microgyria in a... -
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- Aicardi Syndrome: A case report
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Moon JL, Jung KH, Kang SY
- KMID: 2323451
- J Korean Acad Rehabil Med.
- 2000 Jun;24(3):576-581.
Aicardi syndrome is defined by the clinical triad infantile spasms, agenesis of the corpus callosum, and pathognomonic chorioretinal lacunae. Infantile spasm begins at early infancy and tends to be controlled... -
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