Literature DB >> 19793345

A case of ankyloblepharon, ectodermal dysplasia, and cleft lip/palate syndrome with ectrodactyly: are the p63 syndromes distinct after all?

Yvonne E Chiu1, Beth A Drolet, Kelly J Duffy, Kristen E Holland.   

Abstract

Ectodermal dysplasias are diseases with abnormal development of ectodermally derived tissues such as skin, hair, teeth, and nails. Mutations in the transcription factor p63 have been linked to several syndromes characterized by ectodermal, orofacial, and limb defects. We present the case of an infant with ankyloblepharon, cleft palate, scalp dermatitis, and ectrodactyly. She is unique for having a novel p63 mutation that has not been previously reported. Her case also points to the significant overlap between the p63-associated ectodermal dysplasias and challenges the traditional diagnostic schema for these rare syndromes.
© 2009 The Authors. Journal compilation © 2009 Wiley Periodicals, Inc.

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Year:  2011        PMID: 19793345     DOI: 10.1111/j.1525-1470.2009.00976.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  2 in total

1.  Ankyloblepharon Filiforme Adnatum in a Newborn.

Authors:  Giulia Bordin; Enrico Valerio; Mario Cutrone
Journal:  AJP Rep       Date:  2014-12-15

2.  Differentially Expressed Genes in EEC and LMS Syndromes.

Authors:  Wei Yin; Yaling Song; Yangge Du; Zhuan Bian
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240

  2 in total

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