Your browser doesn't support javascript.
loading
A Case of Wolf-Hirschhorn Syndrome with Long Term Survival Diagnosed by Fluorescent In-situ Hybridization (FISH)
Journal of the Korean Pediatric Society ; : 438-443, 2000.
Artículo en Coreano | WPRIM | ID: wpr-130126
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).
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Brazo / Cromosomas Humanos Par 4 / Diagnóstico / Síndrome de Wolf-Hirschhorn / Hipertelorismo / Labio / Discapacidad Intelectual Tipo de estudio: Estudio diagnóstico Límite: Niño / Femenino / Humanos Idioma: Coreano Revista: Journal of the Korean Pediatric Society Año: 2000 Tipo del documento: Artículo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Brazo / Cromosomas Humanos Par 4 / Diagnóstico / Síndrome de Wolf-Hirschhorn / Hipertelorismo / Labio / Discapacidad Intelectual Tipo de estudio: Estudio diagnóstico Límite: Niño / Femenino / Humanos Idioma: Coreano Revista: Journal of the Korean Pediatric Society Año: 2000 Tipo del documento: Artículo