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Related to aplasia cutis congenita: Fetal hydantoin syndrome, sirenomelia
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Words related to aplasia

failure of some tissue or organ to develop

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Aplasia cutis congenita in a newborn: etiopathogenic review and diagnostic approach.
Three siblings with extensive aplasia cutis congenita of the scalp and underlying bone defect: autosomal recessive inheritance.
Aplasia cutis congenita (ACC) (OMIM 107600) is another rare anomaly with congenital localized absence of skin usually on the scalp.
Some cases of aplasia cutis congenita will have a so-called hair collar sign, which is a ring of dark hair that often surrounds a scalp lesion.
1-3 It is a clinical syndrome associated with aplasia cutis congenita (ACC), which is classified into nine groups according to location, hereditary mode and associated anomalies.
Adams-Oliver syndrome has a wide spectrum of anomalies ranging from aplasia cutis congenita, cutis marmorata telangiectatica congenita and transverse limb defects.
a burn reconstructive surgeon at University Hospital and Medical Center at Stony Brook, presented a case study of a newborn child who was treated for Aplasia Cutis Congenita of the trunk, a rare congenital condition characterized by the absence of all layers of skin.
The presence of an initial tense bulla on the vertex scalp suggests a diagnosis of aplasia cutis congenita.