Kindler syndrome: report of two cases

Kindler syndrome: report of two cases

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 Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosensitivity, poikiloderma, cutaneous atrophy and periodontitis.

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Main Authors: Mendes,Luciana, Nogueira,Lisiane, Vilasboas,Virginia, Talhari,Carolina, Talhari,Sinésio, Santos,Mônica
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Dermatologia 2012
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962012000500020
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spelling oai:scielo:S0365-059620120005000202012-10-01Kindler syndrome: report of two casesMendes,LucianaNogueira,LisianeVilasboas,VirginiaTalhari,CarolinaTalhari,SinésioSantos,Mônica Clinical diagnosis Epidermolysis bullosa Photosensitivity disorders Signs and symptoms 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 Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosensitivity, poikiloderma, cutaneous atrophy and periodontitis.info:eu-repo/semantics/openAccessSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia v.87 n.5 20122012-10-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962012000500020en10.1590/S0365-05962012000500020
institution SCIELO
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country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Mendes,Luciana
Nogueira,Lisiane
Vilasboas,Virginia
Talhari,Carolina
Talhari,Sinésio
Santos,Mônica
spellingShingle Mendes,Luciana
Nogueira,Lisiane
Vilasboas,Virginia
Talhari,Carolina
Talhari,Sinésio
Santos,Mônica
Kindler syndrome: report of two cases
author_facet Mendes,Luciana
Nogueira,Lisiane
Vilasboas,Virginia
Talhari,Carolina
Talhari,Sinésio
Santos,Mônica
author_sort Mendes,Luciana
title Kindler syndrome: report of two cases
title_short Kindler syndrome: report of two cases
title_full Kindler syndrome: report of two cases
title_fullStr Kindler syndrome: report of two cases
title_full_unstemmed Kindler syndrome: report of two cases
title_sort kindler syndrome: report of two cases
description 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 Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosensitivity, poikiloderma, cutaneous atrophy and periodontitis.
publisher Sociedade Brasileira de Dermatologia
publishDate 2012
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962012000500020
work_keys_str_mv AT mendesluciana kindlersyndromereportoftwocases
AT nogueiralisiane kindlersyndromereportoftwocases
AT vilasboasvirginia kindlersyndromereportoftwocases
AT talharicarolina kindlersyndromereportoftwocases
AT talharisinesio kindlersyndromereportoftwocases
AT santosmonica kindlersyndromereportoftwocases
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