Hutchinson-Gilford Progeria Syndrome with G608G LMNA Mutation
Journal of Korean Medical Science
; : 1642-1645, 2011.
Article
ي En
| WPRIM
| ID: wpr-112905
المكتبة المسؤولة:
WPRO
ABSTRACT
Hutchinson-Gilford progeria syndrome (HGPS) is a rare condition originally described by Hutchinson in 1886. Death result from cardiac complications in the majority of cases and usually occurs at average age of thirteen years. A 4-yr old boy had typical clinical findings such as short stature, craniofacial disproportion, alopecia, prominent scalp veins and sclerodermatous skin. This abnormal appearance began at age of 1 yr. On serological and hormonal evaluation, all values are within normal range. He was neurologically intact with motor and mental development. An echocardiogram showed calcification of aortic and mitral valves. Hypertrophy of internal layer at internal carotid artery suggesting atherosclerosis was found by carotid doppler sonography. He is on low dose aspirin to prevent thromboembolic episodes and on regular follow up. Gene study showed typical G608G (GGC- > GGT) point mutation at exon 11 in LMNA gene. This is a rare case of Hutchinson-Gilford progeria syndrome confirmed by genetic analysis in Korea.
Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Progeria
/
Prognosis
/
Point Mutation
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Lamin Type A
/
Republic of Korea
نوع الدراسة:
Prognostic_studies
المحددات:
Child, preschool
/
Humans
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Male
البلد/الأقليم حسب الموضوع:
Asia
اللغة:
En
مجلة:
Journal of Korean Medical Science
السنة:
2011
نوع:
Article