Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome.

Abstract:

:Encephalocraniocutaneous lipomatosis (ECCL) is a rare neurocutaneous syndrome that include skin, ocular, and neurological disorders. This study describes the case of a 16-year-old girl that came to observation for the treatment of a congenital alopecia causing great psychological distress. After two expansion procedures the hairless patch was restored with high patient satisfaction. The case met all the criteria for definite diagnosis of ECCL.

journal_name

J Plast Surg Hand Surg

authors

Borgognoni L,Brandani P,Reali F,Gerlini G,Sestini S,Maio V,Reali UM

doi

10.3109/2000656X.2013.842293

subject

Has Abstract

pub_date

2014-12-01 00:00:00

pages

449-51

issue

6

eissn

2000-656X

issn

2000-6764

journal_volume

48

pub_type

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