Literature DB >> 10861677

Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entity.

K Keymolen1, R Van Damme-Lombaerts, A Verloes, J P Fryns.   

Abstract

In 1987 Buttiens and Fryns [1987: Am J Med Genet 27:651-660] reported on two sibs, brother and sister, with severe distal limb defects, micrognathia, and mild to moderate mental retardation. The male also showed severe myopia and oligomeganephronia. To the best of our knowledge, no other similar patients have been described since. We report on a boy with a similar phenotype. . Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10861677

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


  2 in total

1.  Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome.

Authors:  Ali Al Kaissi; Franz Grill; Hatem Safi; Maher Ben Ghachem; Farid Ben Chehida; Klaus Klaushofer
Journal:  Orphanet J Rare Dis       Date:  2007-01-08       Impact factor: 4.123

2.  Acromelia-oligodontia syndrome.

Authors:  Jyothirmai Talasila; Ramaswamy Pachigolla; Kiranmai V S N Yarlagadda; Ramu Vuppala; Karl-Heinz Grzeschik; Sai Kiran K V S; Catherine M Rose; Gary S Gottesman; Zsolt Urban
Journal:  Clin Case Rep       Date:  2017-05-05
  2 in total

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