Literature DB >> 18019373

Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.

L E Becerra-Solano1, M P Casillas-Avila, M Díaz-Rodríguez, J A Nastasi-Catanese, J J Toscano-Flores, M L Ramírez-Dueñas.   

Abstract

We describe a father-son Mexican pair with typical features of Schilbach-Rott syndrome (SRS): ocular hypotelorism, cleft palate, hypospadias (only in the child), and microcephaly. This observation documents for the first time a male to male transmission and therefore confirms that the SRS is inherited as an autosomal dominant trait with variable expressivity.

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Year:  2007        PMID: 18019373

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  1 in total

1.  Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene.

Authors:  Paolo Prontera; Daniela Rogaia; Ester Sallicandro; Amedea Mencarelli; Valentina Imperatore; Gabriella Maria Squeo; Giuseppe Merla; Sandro Elisei; Danilo Moretti-Ferreira; Susanna Esposito; Gabriela Stangoni
Journal:  Eur J Hum Genet       Date:  2019-04-01       Impact factor: 4.246

  1 in total

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