Kindler syndrome: report of two cases Síndrome de Kindler: relato de dois casos

Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindl...

Full description

Bibliographic Details
Main Authors: Luciana Mendes, Lisiane Nogueira, Virginia Vilasboas, Carolina Talhari, Sinésio Talhari, Mônica Santos
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2012-10-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962012000500020