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Two Siblings with Adolescent/Adult Onset Niemann-Pick Disease Type C in Korea
Journal of Korean Medical Science ; : 1168-1172, 2016.
Article in English | WPRIM | ID: wpr-73248
ABSTRACT
Niemann-Pick disease, type C (NP-C), is caused by NPC1 or NPC2 gene mutations. Progressive neurological, psychiatric, and visceral symptoms are characteristic. Here, we present cases of a brother (Case 1) and sister (Case 2) in their mid-20s with gait disturbance and psychosis. For the Case 1, neurological examination revealed dystonia, ataxia, vertical supranuclear-gaze palsy (VSGP), and global cognitive impairment. Case 2 showed milder, but similar symptoms, with cortical atrophy. Abdominal computed tomography showed hepatosplenomegaly in both cases. NPC1 gene sequencing revealed compound heterozygote for exon 9 (c.1552C>T [R518W]) and exon 18 (c.2780C>T [A927V]). Filipin-staining tests were also positive. When a young patient with ataxia or dystonia shows VSGP, NP-C should be considered.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Psychotic Disorders / DNA Mutational Analysis / Membrane Glycoproteins / Carrier Proteins / Tomography, X-Ray Computed / Exons / Gait Disorders, Neurologic / Siblings / Asian People / Abdomen Limits: Female / Humans / Male Country/Region as subject: Asia Language: English Journal: Journal of Korean Medical Science Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Psychotic Disorders / DNA Mutational Analysis / Membrane Glycoproteins / Carrier Proteins / Tomography, X-Ray Computed / Exons / Gait Disorders, Neurologic / Siblings / Asian People / Abdomen Limits: Female / Humans / Male Country/Region as subject: Asia Language: English Journal: Journal of Korean Medical Science Year: 2016 Type: Article