Literature DB >> 22555841

[Waardenburg Syndrome: a review of literature and case reports].

S Salvatore1, C Carnevale, R Infussi, L Arrico, M Mafrici, A M Plateroti, E M Vingolo.   

Abstract

Waadernburg syndrome (WS) is an autosomal dominant disease clinically and genetically heterogeneous. It is characterized by non-progressive sensorineuronal hearing loss of variable degree and anomalous pigmentation (of the eyes, skin and stria vascularis of cochlear duct) caused by melanocytes absence. The syndrome is caused by mutations in genes that regulate the melanocytes differentiation from the neural crest during embriogenetic development. This study will review the literature on WS and explain more in detail the ocular findings in WS, while reporting new findings on two newly diagnosed cases.

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Year:  2012        PMID: 22555841

Source DB:  PubMed          Journal:  Clin Ter        ISSN: 0009-9074


  2 in total

Review 1.  [Piebaldism: a pigmentary anomaly to recognize: about a case and review of the literature].

Authors:  Hajar El Kouarty; Badr Sououd Benjelloun Dakhama
Journal:  Pan Afr Med J       Date:  2016-11-14

2.  Waardenburg syndrome type I: Dental phenotypes and genetic analysis of an extended family.

Authors:  L Sólia-Nasser; S-N de Aquino; L-M R Paranaíba; A Gomes; P Dos-Santos-Neto; R-D Coletta; A-F Cardoso; A-C Frota; H Martelli-Júnior
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2016-05-01
  2 in total

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