A Case of Adams-Oliver Syndrome
Author(s) -
Jong-Keun Seo,
Ju-Hyun Kang,
Hyun-Jae Lee,
Deborah Lee,
Ho-Suk Sung,
Seon-Wook Hwang
Publication year - 2010
Publication title -
annals of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.385
H-Index - 37
eISSN - 2005-3894
pISSN - 1013-9087
DOI - 10.5021/ad.2010.22.1.96
Subject(s) - medicine , genitourinary system , aplasia cutis congenita , organ system , aplasia , dermatology , anatomy , pathology , scalp , disease
Adams-Oliver syndrome (AOS) is a congenital condition characterized by aplasia cutis congenita, transverse limb defects, and cutis marmorata telangiectatica. AOS can also be associated with extensive lethal anomalies of internal organs, including the central nervous, cardiopulmonary, gastrourointestinal, and genitourinary systems. Generally, the more severe these interrelated anomalies are, the poorer the prognosis becomes. In the relevant literature on this topic, it is somewhat unclear as to whether the prognosis of AOS without lethal anomalies alters the lifespan. We report a case of AOS with typical skin defects only, and no internal organ anomalies.
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