Literature DB >> 1776641

Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs.

M Urioste1, A Arroyo, M L Martínez-Frías.   

Abstract

We report on 2 sibs with a similar MCA pattern consisting of generalized lymphedema, cervical lymphocele, shortness of limbs, bowed long bones, and multicystic kidneys with fibrotic liver or pancreas. To our knowledge, this is the second observation of such a combination of defects in sibs, and it confirms the existence of the syndrome reported by Cumming et al. [1986] and its autosomal recessive inheritance.

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Year:  1991        PMID: 1776641     DOI: 10.1002/ajmg.1320410419

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


  1 in total

1.  Acampomelic form of campomelic dysplasia with SOX9 missense mutation.

Authors:  Hariharan Gopakumar; Andrea Superti-Furga; Sheila Unger; Gerd Scherer; P K Rajiv; Sheela Nampoothiri
Journal:  Indian J Pediatr       Date:  2013-04-07       Impact factor: 1.967

  1 in total

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