Literature DB >> 10083645

[The Townes-Brocks syndrome in Spain: the epidemiological aspects in a consecutive series of cases].

M L Martínez-Frías1, E Bermejo Sánchez, I Arroyo Carrera, J L Pérez Fernández, M Pardo Romero, E Burón Martínez, F Hernández Ramón.   

Abstract

INTRODUCTION: Townes-Brocks syndrome is constituted by a multi-systemic pattern of congenital anomalies with autosomal dominant inheritance. The most characteristic defects are those affecting hearing and the auricle, anal atresia and thumb anomalies. PATIENTS AND METHODS: We present the epidemiological characteristics of six cases of Townes-Brocks syndrome identified in the consecutive series of 25,967 malformed live born infants detected among 1,431,368 live births surveyed by the ECEMC (Spanish Collaborative Study of Congenital Malformations) between April 1976 and June 1997. RESULTS AND
CONCLUSIONS: The minimal estimated frequency of Townes-Brocks syndrome in our data is 0.42 cases per 100,000 liveborn infants. These infants have low birth weights. Similar to other published studies, we have observed in our cases a wide variation in the clinical expression of the syndrome, showing great inter-family, as well as intrafamily variability.

Entities:  

Mesh:

Year:  1999        PMID: 10083645

Source DB:  PubMed          Journal:  An Esp Pediatr        ISSN: 0302-4342


  4 in total

1.  Novel mutation in the SALL1 gene in a four-generation Chinese family with uraemia: A case report.

Authors:  Jia-Xi Fang; Jin-Shi Zhang; Min-Min Wang; Lin Liu
Journal:  World J Clin Cases       Date:  2022-07-16       Impact factor: 1.534

2.  Endocrine abnormalities in Townes-Brocks syndrome.

Authors:  Cara Lawrence; Irene Hong-McAtee; Bryan Hall; James Hartsfield; Andrew Rutherford; Tracy Bonilla; Carolyn Bay
Journal:  Am J Med Genet A       Date:  2013-07-25       Impact factor: 2.802

3.  Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.

Authors:  Amira Elmakky; Ilaria Stanghellini; Antonio Landi; Antonio Percesepe
Journal:  Curr Genomics       Date:  2015-08       Impact factor: 2.236

4.  A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants.

Authors:  Javier A López-Rivera; Eduardo Pérez-Palma; Joseph Symonds; Amanda S Lindy; Dianalee A McKnight; Costin Leu; Sameer Zuberi; Andreas Brunklaus; Rikke S Møller; Dennis Lal
Journal:  Brain       Date:  2020-04-01       Impact factor: 13.501

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.