Familial aplasia cutis congenita

Authors

  • Sajad Ahmad Salati

Keywords:

Aplasia cutis congenita, familial, sporadic, graft, bleeding

Abstract

Aplasia cutis is a disorder characterized by developmental absence of portion of skin. Scalp is the most commonly involved site. The etiopathogenesis of the disease is not fully understood and multiple theories have been proposed for explanation. The disorder occurs sporadically and cases with familial occurrence are very rarely mentioned in literature. One such case with familial aplasia cutis of scalp is reported in this article. 

References

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Published

2016-12-15

How to Cite

1.
Salati SA. Familial aplasia cutis congenita. J Pak Assoc Dermatol [Internet]. 2016Dec.15 [cited 2024Dec.7];23(2):221-4. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/347

Issue

Section

Case Reports