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
in English
| 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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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Review Literature as Topic
/
Developmental Disabilities
/
De Lange Syndrome
/
Hypertrichosis
/
Intellectual Disability
Type of study:
Case report
Limits:
Female
/
Humans
Language:
English
Journal:
J. Pak. Assoc. Dermatol.
Year:
2011
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