Adams-Oliver Syndrome: A Case With Full Expression
Author(s) -
Amir Dehdashtian,
Masoud Dehdashtian
Publication year - 2016
Publication title -
pediatric reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.297
H-Index - 19
ISSN - 2036-7503
DOI - 10.4081/pr.2016.6517
Subject(s) - aplasia cutis congenita , medicine , scalp , aplasia , abnormality , cutis laxa , trunk , weight gain , ectodermal dysplasia , dermatology , pediatrics , anatomy , body weight , ecology , psychiatry , biology
Adams-Oliver syndrome (AOS) is characterized by the combination of congenital scalp defects (aplasia cutis congenita) and terminal transverse limb defects of variable severity. It is believed that Adams-Oliver syndrome without major organ abnormalities does not necessarily alter the normal lifespan. We present a case without detectable major organ abnormality contrary to life but with poor weight gain. A male infant with scalp and skin cutis aplasia, generalized cutis aplasia, dilated veins over scalp and trunk, hypoplastic toes and nails of feet, glaucoma, poor feeding and poor weight gain. This report shows a case of AOS without major multiple organ abnormalities but with poor feeding and abnormal weight gain that may be alter the normal lifespan
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