Aplasia cutis congenita in two brothers - a rare occurence
JPAD-Journal of Pakistan Association of Dermatologists. 2005; 15 (3): 275-277
in English
| IMEMR
| ID: emr-72536
ABSTRACT
Aplasia cutis congenita [ACC] is characterized by the absence of a portion of skin in a localized or widespread area at birth. It is a rare disorder with a complicated pattern of inheritance. No unifying theory can account for all lesions of ACC. Apart from the isolated finding of aplasia cutis; several reports have associated it with a large number of developmental anomalies. Therefore, a complete physical examination should be performed to search for associated physical anomalies or recognizable malformation syndromes. We document two brothers aged, 6 years and I year, who presented with aplasia cutis congenita at almost the same location on scalp
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Skin Abnormalities
/
Ectodermal Dysplasia
/
Siblings
Type of study:
Case report
Limits:
Humans
/
Male
Language:
English
Journal:
J. Pak. Assoc. Dermatol.
Year:
2005
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