Literature DB >> 3180506

A new family with the Townes-Brocks syndrome.

M A de Vries-Van der Weerd1, P J Willems, H M Mandema, L P ten Kate.   

Abstract

We describe a new family with the Townes-Brocks syndrome, a dominantly inherited syndrome of anal, urorenal, ear and limb malformations. The proband shows the full spectrum of anomalies, including imperforate anus, prominent perineal raphe, rectoperineal fistula, triphalangeal thumb, preaxial hexadactyly, syndactyly, clinodactyly, preauricular protuberances, hypoplastic satyr ears, sensorineural hearing loss and urorenal anomalies. In contrast, the father shows only limb anomalies, sensorineural hearing loss and renal anomalies. Anorectal malformations, which are present in almost every patient with the Townes-Brocks syndrome, were absent in the father. This case report illustrates the intrafamilial variability of the Townes-Brocks syndrome. Consequently, careful examination of relatives of patients with this syndrome is necessary for the differential diagnosis with the sporadically inherited VA(C)TER(L) association.

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Year:  1988        PMID: 3180506     DOI: 10.1111/j.1399-0004.1988.tb02862.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  10 in total

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2.  Townes-Brocks syndrome.

Authors:  R König; U Schick; S Fuchs
Journal:  Eur J Pediatr       Date:  1990-12       Impact factor: 3.183

Review 3.  Townes-Brocks syndrome.

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

4.  The Townes-Brocks syndrome.

Authors:  M O'Callaghan; I D Young
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5.  Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

Authors:  J Kohlhase; P E Taschner; P Burfeind; B Pasche; B Newman; C Blanck; M H Breuning; L P ten Kate; P Maaswinkel-Mooy; B Mitulla; J Seidel; S J Kirkpatrick; R M Pauli; D S Wargowski; K Devriendt; W Proesmans; O Gabrielli; G V Coppa; E Wesby-van Swaay; R C Trembath; A A Schinzel; W Reardon; E Seemanova; W Engel
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Review 6.  The role of stem cell factor SALL4 in leukemogenesis.

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7.  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
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8.  An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.

Authors:  A J Green; R N Sandford; B C Davison
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

9.  Hypertrophy of the raphe perinei in male infants.

Authors:  T James
Journal:  J R Soc Med       Date:  1991-12       Impact factor: 18.000

10.  Phenotypic and genotypic aspects of Townes-Brock syndrome: case report of patient in southern Brazil with a new SALL1 hotspot region nonsense mutation.

Authors:  Paulo Breno Noronha Liberalesso; Mara L Cordeiro; Simone Carreiro Vieira Karuta; Karyn Regina Jordão Koladicz; Anderson Nitsche; Bianca Simone Zeigelboim; Salmo Raskin; Michael Rauchman
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  10 in total

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