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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  • EP ID EP587588
  • DOI -
  • Views 142
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How To Cite

Dr. Rakesh Kotha, Dr. Arjun Jadhao, Dr. Himabindu Singh, Dr. Paramesh Pandala, Dr. Nandini Mounika (2018). Aplasia cutis congenital type 6 A rare type- a case report. International Journal of Medical and Health Research, 4(9), 30-31. https://europub.co.uk/articles/-A-587588