Literature DB >> 2309763

Carpenter syndrome: marked variability of expression to include the Summitt and Goodman syndromes.

R Gershoni-Baruch1.   

Abstract

Here we report on two sibs with Carpenter syndrome showing marked intrafamilial variability. One patient had craniosynostosis of the sagittal suture, normal intelligence, and no abnormalities of hands and feet. The second patient had polysyndactyly of hands and feet, normal intelligence, and no craniosynostosis. The diagnosis of Carpenter syndrome was made after the second affected child in the family was born. This report emphasizes previous suggestions that acrocephalopolysyndactyly, type II, has variable clinical expression. It is suggested that polysyndactyly of feet is not an absolute requisite for the diagnosis of Carpenter syndrome. This allows the inclusion of Summitt and Goodman syndromes within the clinical spectrum of this disorder.

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Year:  1990        PMID: 2309763     DOI: 10.1002/ajmg.1320350218

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Transabdominal embryoscopy for the detection of Carpenter syndrome during the first trimester.

Authors:  N A Ginsberg; D Zbaraz; C Strom
Journal:  J Assist Reprod Genet       Date:  1994-08       Impact factor: 3.412

Review 2.  Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis.

Authors:  Federica Tiberio; Ornella Parolini; Wanda Lattanzi
Journal:  Genes (Basel)       Date:  2021-07-14       Impact factor: 4.096

  2 in total

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