- Treatment of Psychiatric Symptoms in a Patient with Neuroacanthocytosis: A Case Report
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Hwang HR, Kim JJ
- KMID: 2287479
- Korean J Psychopharmacol.
- 2012 Jan;23(1):36-39.
Neuroacanthocytosis is a rare hereditary disorder characterized by various neurological symptoms and the presence of abnormal red blood cell called acanthocytosis. Degeneration of striatum, which accounts for characteristic motor and... -
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- The First Genetically Confirmed McLeod Syndrome in Korea
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Park KW, Jeong S, Seo EJ, Lee CS
- KMID: 2379308
- J Korean Neurol Assoc.
- 2017 May;35(2):85-88.
- doi: 10.17340/jkna.2017.2.4
McLeod syndrome is a rare X-linked multisystem disorder which forms the core of neuroacanthocytosis syndrome. Neurological symptoms characterized by chorea, seizure, cognitive impairment, and psychosis mostly develop around the 5-6th... -
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- A Case of Fly Catcher's Tongue Phenomenon in Hallervorden-Spatz Disease
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Ha CK, Kang SY, Rha JH, Lee IK
- KMID: 2186061
- J Korean Neurol Assoc.
- 2000 Mar;18(2):255-257.
Hallervorden-Spatz disease (HSD) is a rare, progressive, autosomal recessive hereditary disorder characterized by pyramidal and extrapyramidal signs, speech disturbances, mental deterioration and retinal degeneration during childhood or adolescence. In late-onset... -
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- Neuroacanthocytosis: 2 Cases of Familial Choreoacanthocytosis
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Lee SB, Park SC, Lee MS
- KMID: 1957242
- J Korean Neurol Assoc.
- 1995 Sep;13(3):651-656.
Neuroacanthocytosis is a rare dosorder characterized by various neurological manifestations and the presence of abnormal red blood cells called acanthocytes which have a disturbed morphology showing spiky, knobby end projections.... -
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- Acanthocytosis in a Patient with Chorea-acanthocytosis
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Lee SM, Lee JH
- KMID: 2312203
- Lab Med Online.
- 2012 Jul;2(3):179-180.
No abstract available. -
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- Globus Pallidus Interna Deep Brain Stimulation for Chorea-Acanthocytosis
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Lee JH, Cho WH, Cha SH, Kang DW
- KMID: 2191199
- J Korean Neurosurg Soc.
- 2015 Feb;57(2):143-146.
- doi: 10.3340/jkns.2015.57.2.143
Chorea-acanthocytosis (ChAc) is a rare hereditary disorder characterized by involuntary choreiform movements and erythrocytic acanthocytosis. Pharmacotherapy for control of involuntary movements has generally been of limited benefit. Deep brain stimulation... -
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- A Familial Case of Choreoacanthocytosis
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Shin BS, Song DW, Lee SH, Seo MW, Kim YH
- KMID: 1659737
- J Korean Neurol Assoc.
- 1996 Dec;14(4):1000-1006.
We have experienced a family case of 3 sisters in whom the proband showed a complete form of the choreo-acanthosytosis. 439-year-old female proband was admitted because of frequent seizures. She... -
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