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Adams-Oliver Syndrome. A case with isolated aplasia cutis congenita and skeletal defects
Ola Bakry1, Abdalla Attia, Eman Nabil El Shafey
1Department of Dermatology, Andrology and S.T.Ds, Faculty of Medicine, Menoufiya University, Menoufiya 32511, Egypt.
Background:
Adams-Oliver Syndrome is characterized by the combination of aplasia cutis congenita and limb anomalies. It was initially described in 1945 by Adams and Oliver.
Main Observations:
We report a case of a 10-year-old girl with Adams-Oliver Syndrome with aplasia cutis congenita and limb defects only with no internal organ anomalies.
Conclusions:
Adams-Oliver Syndrome is a rare multisystem disorder of unknown etiology. It may be presented by isolated aplasia cutis congenita and limb anomalies.
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