Aplasia cutis congenital type 6 A rare type- a case report
Journal Title: International Journal of Medical and Health Research - Year 2018, Vol 4, Issue 9
Abstract
Aplasia cutis congenita is a heterogenous group of disorders where localized absence of skin particularly scalp and associated anomalies were present. It has several types. Most common one is type 1. Here we are presenting a rare case type 6 also known as Bart syndrome. It has good prognosis if proper medical management is done and if not associated with any other anomalies
Authors and Affiliations
Dr. Rakesh Kotha, Dr. Arjun Jadhao, Dr. Himabindu Singh, Dr. Paramesh Pandala, Dr. Nandini Mounika
Keywords
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