Literature DB >> 2624264

New type of autosomal recessive short-limb dwarfism with absent fibulae, exceptionally short digits, and normal intelligence.

G Kohn1, M Veder, A Schoenfeld, R el Shawwa.   

Abstract

Short-limb dwarfism is of heterogeneous origin and has various clinical manifestations. This communication describes a previously apparently unreported type of short-limb dwarfism in 3 affected sibs. Characteristics of this syndrome are bilateral absence of fibulae and severe abnormalities of all digits.

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Year:  1989        PMID: 2624264     DOI: 10.1002/ajmg.1320340416

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


  1 in total

1.  Prenatal diagnosis of type 1 fibular hemimelia.

Authors:  Zeynep Ilerisoy Yakut; Ali Ipek; Hatice Akkaya; Halil Arslan
Journal:  J Med Ultrason (2001)       Date:  2014-07-16       Impact factor: 1.314

  1 in total

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