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A Case of Aplasia Cutis Congenita, Type V
Annals of Dermatology ; : 73-76, 1997.
Article in English | WPRIM | ID: wpr-25053
ABSTRACT
Aplasia cutis congenita is a congenital localized or widespread absence of the skin. We report a case of aplasia cutis congenita, type V, in a 6-day-old male infant born with the stellate and linear skin lesions covered by granulation tissue and soft capsule with slightly elevated erythematous edges on the trunk and lower extremities without any associated family history. The patient had amniotic bands and were diagnosed as aplasia cutis, type V. The patient received conservative treatment such as antiseptic dressing and prophylactic systemic antibiotics with healing of the ulcer.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Bandages / Ulcer / Ectodermal Dysplasia / Lower Extremity / Granulation Tissue / Amniotic Band Syndrome / Anti-Bacterial Agents Limits: Humans / Infant / Male / Infant, Newborn Language: English Journal: Annals of Dermatology Year: 1997 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Bandages / Ulcer / Ectodermal Dysplasia / Lower Extremity / Granulation Tissue / Amniotic Band Syndrome / Anti-Bacterial Agents Limits: Humans / Infant / Male / Infant, Newborn Language: English Journal: Annals of Dermatology Year: 1997 Type: Article