Cornelia de Lange syndrome - a cause of hypertrichosis in children: case report and review of literature
JPAD-Journal of Pakistan Association of Dermatologists. 2011; 21 (3): 211-214
en Inglés
| IMEMR
| ID: emr-137431
ABSTRACT
Cornelia de Lange syndrome is a rare developmental disorder characterized by hypertrichosis, low intelligence, delayed milestones and skeletal and dental abnormalities. Gastroesophageal dysfunction, ophthalmologic, cardiac and genitourinary anomalies, learning difficulties, and mental retardation may be present in severe cases. We report a case of this syndrome who presented for laser treatment for the problem of hypertrichosis, and on examination other features of the syndrome were noted
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Literatura de Revisión como Asunto
/
Discapacidades del Desarrollo
/
Síndrome de Cornelia de Lange
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Hipertricosis
/
Discapacidad Intelectual
Tipo de estudio:
Informe de Casos
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
J. Pak. Assoc. Dermatol.
Año:
2011
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