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Hereditary Aplasia Cutis Congenita and Associated DefectsThree Instances in One Family and a Survey of Reported CasesUniversity Affiliated Cincinnati Center for Developmental Disorders and the Children's Hospital Medical Center, University of Cincinnati College of Medicine
University Affiliated Cincinnati Center for Developmental Disorders and the Children's Hospital Medical Center, University of Cincinnati College of Medicine
University Affiliated Cincinnati Center for Developmental Disorders and the Children's Hospital Medical Center, University of Cincinnati College of Medicine
University Affiliated Cincinnati Center for Developmental Disorders and the Children's Hospital Medical Center, University of Cincinnati College of Medicine Hereditary aplasia cutis congenita (ACC) is a rare, dominantly inherited syndrome of scalp aplasia associated with defects of the underlying skull and absent distal phalanges of the feet. The scalp lesions are generally benign, but the increased risk of bleeding or meningitis may require skin grafting.
Clinical Pediatrics, Vol. 16, No. 7,
610-614 (1977) This article has been cited by other articles:
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