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KMID : 1039920210280010048
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Neonatal Medicine
2021 Volume.28 No. 1 p.48 ~ p.52
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Case of Mental Retardation Associated with Aplasia Cutis Congenita and Skull Defect
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Cho Hyun-Chul
Hwang Jong-Hee
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Abstract
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Aplasia cutis congenita (ACC) is a rare congenital disorder characterized by skin defects involving the epidermis, dermis, subcutaneous tissue, bone, and sometimes dura. It commonly affects the scalp in approximately 70% of cases, but the neck, trunk, and the extremities can also be affected. ACC can occur either as an isolated condition or associated with other anomalies and congenital syndromes, and it can be acquired either genetically or sporadically. Morbidity and mortality are associated with the defects of skull bone, dura, and other multiple anomalies. We herein report the case of a female infant, with a large scalp defect accompanied by a skull defect noted at birth, who developed mental retardation in the preschool years.
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KEYWORD
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Ectodermal dysplasia, Scalp dermatoses, Parietal bone, Infants
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