Aplasia cutis congenita and amniotic band syndrome: an uncommon association

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منابع مشابه

Aplasia cutis congenita and amniotic band syndrome: an uncommon association.

To cite: Pimenta J, Lapa P, Ramos L. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016218950 DESCRIPTION Amniotic band syndrome is an unusual clinical entity with a wide variety of presentations that include constriction rings, syndactyly and limb or digital amputations. 2 Aplasia cutis congenita is a rare congenital anomaly involving variant layers of the skin...

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Aplasia cutis congenita

The patient was a female neonate bornprematurely at 36 weeks of gestation by a Cesareansection. During pregnancy, the mother had nohistory of fever, drug use, or X-ray exposure.The mother was gravida 2 and had no history ofabortion. Her first child was healthy. There wasno record of birth trauma. The perinatal historywas negative for intrauterine trauma, the use ofantithyroid medication, or mis...

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Type VI Aplasia Cutis Congenita: Bart's Syndrome

Bart's syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart's syndrome (BS) is diagnosed clinically based on the disorder's unique signs and symptoms but histologic evaluation of the skin can help to confirm the final d...

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Aplasia 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...

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Aplasia cutis congenita.

Two cases of aplasia cutis congenita are reported here. One of the cases also had pre- and postaxial polydactyly and other digital anomalies.

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ژورنال

عنوان ژورنال: BMJ Case Reports

سال: 2017

ISSN: 1757-790X

DOI: 10.1136/bcr-2016-218950