Literature DB >> 24902757

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

C Tziotzios1, G Petrof, L Liu, A Verma, E K Wedgeworth, J E Mellerio, J A McGrath.   

Abstract

BACKGROUND: Schöpf-Schulz-Passarge syndrome (SSPS) is an autosomal recessive form of ectodermal dysplasia resulting from mutations in WNT10A.
OBJECTIVES: To document the spectrum of clinical features and search for pathogenic mutations in seven unrelated cases of SSPS.
METHODS: Clinical examination of patients and Sanger sequencing of genomic DNA spanning the coding exons and flanking spice sites of WNT10A.
RESULTS: Most subjects had bilateral eyelid cysts and some degree of palmoplantar keratoderma, although nail, hair, and teeth abnormalities were variably present. Bi-allelic pathogenic mutations in WNT10A were found in all seven subjects. New mutations comprised p.Glu390*, p.Ser270Arg, and p.Cys362Arg; the recurrent mutations were p.Cys107* and p.Ala131Thr.
CONCLUSIONS: This study reveals the range of ectodermal pathology in cases of SSPS that result from WNT10A mutations. Eyelid cysts provide a useful clinical clue to diagnosing SSPS which may be less rare than is currently appreciated.
© 2014 British Association of Dermatologists.

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Year:  2014        PMID: 24902757     DOI: 10.1111/bjd.13158

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  4 in total

1.  Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz.

Authors:  Karola Maria Stieler; Theodosia Bartzela; Christian Finke; Ulrike Blume-Peytavi; Judith Fischer
Journal:  Acta Derm Venereol       Date:  2020-07-28       Impact factor: 3.875

2.  Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation.

Authors:  Anne Bruun Krøigård; Ole Clemmensen; Hans Gjørup; Jens Michael Hertz; Anette Bygum
Journal:  BMC Dermatol       Date:  2016-03-10

3.  Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.

Authors:  Birgitta Bergendal; Johanna Norderyd; Xiaolei Zhou; Joakim Klar; Niklas Dahl
Journal:  BMC Med Genet       Date:  2016-11-24       Impact factor: 2.103

4.  WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation.

Authors:  Mingang Xu; Jeremy Horrell; Melinda Snitow; Jiawei Cui; Heather Gochnauer; Camille M Syrett; Staci Kallish; John T Seykora; Fei Liu; Dany Gaillard; Jonathan P Katz; Klaus H Kaestner; Brooke Levin; Corinne Mansfield; Jennifer E Douglas; Beverly J Cowart; Michael Tordoff; Fang Liu; Xuming Zhu; Linda A Barlow; Adam I Rubin; John A McGrath; Edward E Morrisey; Emily Y Chu; Sarah E Millar
Journal:  Nat Commun       Date:  2017-06-07       Impact factor: 14.919

  4 in total

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