Literature DB >> 19697429

Pathologic changes of skin and hair in ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.

Megan K Dishop1, Alanna F Bree, M John Hicks.   

Abstract

Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome is a rare disorder of hair, skin, nails, and dentition caused by mutations in the p63 gene. Pathologic changes of skin and hair in AEC syndrome have previously been described in isolated case reports. Biopsies of normal and lesional skin from 19 patients with AEC syndrome were examined by light microscopy. Hair samples from 18 patients were examined by light and scanning electron microscopy. Histopathologic changes identified within the skin biopsies from clinically unaffected skin include mild atrophy, focal orthokeratosis, and mild superficial perivascular lymphocytic dermatitis. Scattered melanophages in the superficial and deep dermis likely reflect post-inflammatory change. One patient with a unilateral eruption of monomorphic papulopustules on the chest and shoulder demonstrated an acneiform intraepidermal pustule. Examination of the hair shafts revealed atrophy and loss of melanin pigment in some of the patients. Structural abnormalities included pili torti, pili trianguli et canaliculi, and irregular indentation and shallow grooves. Skin and hair findings in AEC syndrome were found to be generally similar to those described in other ectodermal dysplasia syndromes and corroborates the few prior descriptions in AEC syndrome specifically. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19697429     DOI: 10.1002/ajmg.a.32826

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  5 in total

1.  International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.

Authors:  Mary Fete; Hans vanBokhoven; Suzanne E Clements; Frank McKeon; Dennis R Roop; Maranke I Koster; Caterina Missero; Laura D Attardi; Vivian A Lombillo; Edward Ratovitski; Meena Julapalli; Derek Ruths; Virginia P Sybert; Elaine C Siegfried; Alanna F Bree
Journal:  Am J Med Genet A       Date:  2009-09       Impact factor: 2.802

Review 2.  Modeling AEC-New approaches to study rare genetic disorders.

Authors:  Peter J Koch; Jason Dinella; Mary Fete; Elaine C Siegfried; Maranke I Koster
Journal:  Am J Med Genet A       Date:  2014-03-24       Impact factor: 2.802

3.  p63 control of desmosome gene expression and adhesion is compromised in AEC syndrome.

Authors:  Giustina Ferone; Maria Rosaria Mollo; Helen A Thomason; Dario Antonini; Huiqing Zhou; Raffaele Ambrosio; Laura De Rosa; Domenico Salvatore; Spiro Getsios; Hans van Bokhoven; Jill Dixon; Caterina Missero
Journal:  Hum Mol Genet       Date:  2012-10-29       Impact factor: 6.150

4.  Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndrome.

Authors:  Giustina Ferone; Helen A Thomason; Dario Antonini; Laura De Rosa; Bing Hu; Marica Gemei; Huiqing Zhou; Raffaele Ambrosio; David P Rice; Dario Acampora; Hans van Bokhoven; Luigi Del Vecchio; Maranke I Koster; Gianluca Tadini; Bradley Spencer-Dene; Michael Dixon; Jill Dixon; Caterina Missero
Journal:  EMBO Mol Med       Date:  2012-01-13       Impact factor: 12.137

5.  Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.

Authors:  M Tajir; J Lyahyai; S Guaoua; M El Alloussi; A Sefiani
Journal:  Balkan J Med Genet       Date:  2020-08-26       Impact factor: 0.519

  5 in total

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