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A Case of Wolf-Hirschhorn Syndrome with Long Term Survival Diagnosed by Fluorescent In-situ Hybridization (FISH)
Article in Korean | WPRIM (Western Pacific) | ID: wpr-130126
Responsible library: WPRO
ABSTRACT
Wolf-Hirschhorn syndrome is a multiple malformation syndrome associated with mental and developmental retardation, resulting from a deletion at the short arm of chromosome 4 (4p16.3). We report a 11-year-old girl with Wolf-Hirschhorn syndrome, who was presented with severe growth and mental retardation along with characteristic features-frontal bossing, hypertelorism, downslanting of the palpebral fissures and fishlike lips. The diagnosis was confirmed by fluorescent in-situ hybridization (FISH).
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Arm / Chromosomes, Human, Pair 4 / Diagnosis / Wolf-Hirschhorn Syndrome / Hypertelorism / Lip / Intellectual Disability Type of study: Diagnostic study Limits: Child / Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 2000 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Arm / Chromosomes, Human, Pair 4 / Diagnosis / Wolf-Hirschhorn Syndrome / Hypertelorism / Lip / Intellectual Disability Type of study: Diagnostic study Limits: Child / Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 2000 Document type: Article
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