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ADAMS‐OLIVER SYNDROME: APLASIA CUTIS CONGENITA, TERMINAL TRANSVERSE LIMB DEFECTS AND CUTIS MARMORATA TELANGIECTATICA CONGENITA
Author(s) -
DyallSmith Delwyn,
Ramsden Andrew,
Laurie Simon
Publication year - 1994
Publication title -
australasian journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.67
H-Index - 53
eISSN - 1440-0960
pISSN - 0004-8380
DOI - 10.1111/j.1440-0960.1994.tb01794.x
Subject(s) - aplasia cutis congenita , medicine , scalp , cutis laxa , surgery , dermatology , anatomy
SUMMARY A male infant with the features of Adams‐Oliver syndrome is described. These features included severe aplasia cutis congenita (ACC) of the scalp involving both skin and cranium, a shortened right foot with talipes equinovarus, extensive cutis marmorata telangiectatica congenita and also haemangiomas and ulceration of the abdominal skin. Exposure of the dural membrane was associated with infection, hyponatraemia and finally localised necrosis with herniation of brain and fatal cerebral haemorrhage.