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Aplasia Cutis Congenita, Cleft Palate, Epidermolysis Bullosa, and Ectrodactyly: A New Syndrome?
Author(s) -
Jones Evelyn M.,
Hersh Joseph H.,
Yusk Janice W.
Publication year - 1992
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/j.1525-1470.1992.tb00351.x
Subject(s) - aplasia cutis congenita , medicine , ectrodactyly , epidermolysis bullosa , dermatology , ectodermal dysplasia , scalp
Aptasia cutis congenita (ACC) is a skin disorder in which localized or widespread areas of skin are absent at birth. It has been associated with numerous anomalles and recognizable syndromes. We report a newborn infant with ACC of the scalp, multiple facial abnormalities including cleft palate but not cleft lip, hypoplasia of the distal phalanges of the hands, ectrodactyly of the feet, and epidermolysis bullosa of the extremities and lower trunk. Although this patient had some features that overlapped with ectrodactyly‐ectodermal dysplasia‐clefting syndrome, the absence of cleft lip and presence of additional skin abnormalities made that diagnosis unlikely. This could represent a newly recognized syndrome of numerous malformations in which ACC is associated with a constellation of previously undescribed structural anomalies.

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