Isolated bilateral symmetrical aplasia cutis congenita of lower limbs in a newborn: A rare entity
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چکیده
منابع مشابه
Aplasia Cutis Congenita of Scalp and Back: A Rare Entity
Citation: Sekhon V. Aplasia Cutis Congenita of Scalp and Back: A Rare Entity. Ann Clin Case Rep. 2017; 2: 1367. ISSN: 2474-1655 Copyright © 2017 Sekhon V. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Case Report Published: 05 J...
متن کاملAplasia cutis congenita: a rare extensive bilateral case of extremities
Aplasia cutis congenital is a rare congenital absence of skin, exceptionally involves extremities. Most cases are sporadic but familial autosomal dominant pattern can be found. The etiology remains unclear, both genetic and environmental causes have been implicated. This lesion has primarily a clinical diagnosis. Imaging studies may be used to evaluate underlying tissues and investigate other c...
متن کاملAplasia cutis congenita: a case report
Aplasia cutis congenita is the congenital absence of skin mostcommonly affecting the scalp. No definite etiology is available butmultiple causes such as intrauterine infection, fetal exposure tococaine, heroin, alcohol or antithyroid drugs, vascular disruption,genetic causes, syndromes and teratogens have been suggested.We present an infant with extensive aplasia cutis of the trunk andthigh. He...
متن کاملa rare case of aplasia cutis congenita.
aplasia cutis congenita is a rare anomaly presenting with the absence of skin. no definite etiology is available. the most common site is the scalp. we present an instance with acc occurring symmetrically in both sides of the body from chest to flank.
متن کاملRecessive aplasia cutis congenita of the limbs.
Six inbred persons (five males and one female) in three generations of a single family are reported as having simple congenital absence of skin on the upper or lower limbs or both. The data suggest an autosomal recessive pattern of inheritance for this apparently new clinical entity.
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ژورنال
عنوان ژورنال: International Journal of Clinical Obstetrics and Gynaecology
سال: 2020
ISSN: 2522-6614,2522-6622
DOI: 10.33545/gynae.2020.v4.i2c.520