Literature DB >> 955638

The G syndrome. A four-generation family study.

I L Pedersen, M Mikkelsen, J Oster.   

Abstract

A male infant with hypertelorism, hypospadias, swallowing difficulties with tendency to regurgitation and cough, high arched palate, and a delicate voice, consistent with the G syndrome, is reported. In the family the same symptoms in addition to cleft lip and palate were known in several family members through four generations. In the females only slight manifestations of the syndrome were found, and in the males variable expression of symptoms was observed. Autosomal dominant inheritance is likely, but X-linked inheritance cannot be ruled out.

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Year:  1976        PMID: 955638     DOI: 10.1159/000152784

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  1 in total

1.  Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia.

Authors:  G N Wilson; W J Oliver
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

  1 in total

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