Literature DB >> 21078104

ADULT syndrome caused by a mutation previously associated with EEC syndrome.

Emily Avitan-Hersh1, Margarita Indelman, Reuven Bergman, Eli Sprecher.   

Abstract

Acro-Dermato-Ungual-Lacrimal-Tooth (ADULT) syndrome is a rare autosomal dominant syndrome characterized by ectrodactyly or syndactyly, excessive freckling and dry skin, dysplastic nails, lacrimal duct atresia, primary hypodontia and early loss of permanent teeth. ADULT syndrome is one of five such syndromes that result from mutations in TP63, encoding the transcription factor p63. Until now, only four families and three individuals with ADULT syndrome have been reported in the English literature. We present a 14-year-old female patient with ADULT syndrome and discuss phenotype-genotype correlations in the p63 syndromes.
© 2010 Wiley Periodicals, Inc.

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Year:  2010        PMID: 21078104     DOI: 10.1111/j.1525-1470.2010.01131.x

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


  7 in total

1.  ADULT Phenotype and rs16864880 in the TP63 Gene: Two New Cases and Review of the Literature.

Authors:  Tânia Kawasaki de Araujo; Elaine Lustosa-Mendes; Ana P Dos Santos; Miriam Coelho Molck; Roberta Mazzariol Volpe-Aquino; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-04-13

2.  Ectrodactyly-ectodermal dysplasia clefting syndrome (EEC syndrome).

Authors:  Monika Koul; Rahul Dwivedi; Vinod Upadhyay
Journal:  J Oral Biol Craniofac Res       Date:  2014-08-27

Review 3.  Genetic determinants of syndactyly: perspectives on pathogenesis and diagnosis.

Authors:  Afraah Cassim; Dineshani Hettiarachchi; Vajira H W Dissanayake
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

4.  Ectrodactyly, Ectodermal Dysplasia, Cleft Lip, and Palate (EEC Syndrome) with Tetralogy of Fallot: A Very Rare Combination.

Authors:  Deepak Sharma; Chetan Kumar; Sanjay Bhalerao; Aakash Pandita; Sweta Shastri; Pradeep Sharma
Journal:  Front Pediatr       Date:  2015-06-16       Impact factor: 3.418

5.  A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome.

Authors:  Leandro Ucela Alves; Eliete Pardono; Paulo A Otto; Regina Célia Mingroni Netto
Journal:  Genet Mol Biol       Date:  2014-03-17       Impact factor: 1.771

6.  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

7.  Intermediate Phenotype between ADULT Syndrome and EEC Syndrome Caused by R243Q Mutation in TP63.

Authors:  Yuki Otsuki; Koichi Ueda; Chisei Satoh; Ryuta Maekawa; Koh-Ichiro Yoshiura; Sachiko Iseki
Journal:  Plast Reconstr Surg Glob Open       Date:  2016-12-22
  7 in total

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