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Adams–Oliver Syndrome: A Case Report
Author(s) -
Frantz Jeanine Aparecida Magno,
Lehmkuhl Rafaela Ludvig,
Leitis Lucas Hummelgen,
Uliano Vanessa Golfetto,
Siementcoski Guilherme Antonio
Publication year - 2014
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/pde.12423
Subject(s) - medicine , aplasia cutis congenita , facial dysmorphism , congenital disorder , dermatology , aplasia , cutis laxa , anatomy , surgery , scalp , genetics , gene , phenotype , biology
We report the case of an infant with A dams– O liver syndrome, a rare disorder characterized by aplasia cutis congenita, defects of the limbs and extremities, and cutis marmorata telangiectatica. Other associated anomalies have been reported, such as facial dysmorphism, heart defects, and disorders of the central nervous system.