Literature DB >> 7640757

[Clinical heterogeneity of Townes-Brocks syndrome].

P Parent1, M Bensaid, H Le Guern, A Colin, L Broussine, A Chabarot, A Cozic, B Jehannin, L de Parscau.   

Abstract

BACKGROUND: Townes-Brocks syndrome (TBS) is a rare autosomal dominant entity mainly characterized by ano-rectal, ear and extremities abnormalities with variable clinical expression. CASE REPORTS: The first case had ear and extremities, but not anorectal, abnormalities; a Pierre-Robin sequence with esophageal atresia was also observed. The second case had the classical triad of abnormalities also associated with tetralogy of Fallot which has been only once reported in the literature.
CONCLUSIONS: Both cases are other examples of the frequent clinical variability observed in this syndrome explaining diagnostic difficulties in the absence of a specific marker.

Entities:  

Mesh:

Year:  1995        PMID: 7640757     DOI: 10.1016/0929-693x(96)81200-0

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  2 in total

Review 1.  Townes-Brocks syndrome.

Authors:  C M Powell; R C Michaelis
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

2.  A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the SALL1 gene.

Authors:  Won Ik Choi; Ji Hye Kim; Han Wook Yoo; Sung Hee Oh
Journal:  Korean J Pediatr       Date:  2010-12-31
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.