Literature DB >> 3943255

Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL association.

J H Hersh, M Jaworski, R E Solinger, B Weisskopf, J Donat.   

Abstract

An 8-year-old male is presented with clinical findings of Townes syndrome in an otherwise unaffected family. Additional abnormalities possibly representing low frequency associations of this autosomal dominant multiple malformation syndrome included a cardiac defect and hypospadias. Similarities exist between Townes syndrome and VACTERL association, which is generally regarded to be sporadic in nature. Recognition of Townes syndrome as a distinct entity is critical for implementing appropriate management in early childhood, including amplification of hearing impairments. Variable expressivity may occur in this disorder. Careful evaluation must be made, therefore, of the parents of an affected infant with an apparent sporadic case, in order to provide the couple with an accurate recurrence risk at genetic counseling.

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Year:  1986        PMID: 3943255     DOI: 10.1177/000992288602500209

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  4 in total

1.  Townes-Brocks syndrome.

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

Review 2.  Townes-Brocks syndrome.

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

3.  The Townes-Brocks syndrome.

Authors:  M O'Callaghan; I D Young
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

4.  TOWNES-BROCKS SYNDROME: REPORT OF THREE ADDITIONAL PATIENTS WITH PREVIOUSLY UNDESCRIBED RENAL AND CARDIAC ABNORMALITIES.

Authors:  Amin Y Barakat; Merlin G Butler; James E Salter; Agnes Fogo
Journal:  Dysmorphol Clin Genet       Date:  1988
  4 in total

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