Literature DB >> 6279340

Present nosology of the Cenani-Lenz type of syndactyly.

R A Pfeiffer, M Meisel-Stosiek.   

Abstract

Synostoses of the carpals and metacarpals with oligodactyly were noted in a man whose brother was similarly affected. Since the proband's two children are normal, autosomal recessive transmission is probable. Although abnormalities of the feet, and particularly radioulnar synostosis, are lacking, this malformation is comparable to the Cenani-Lenz type of syndactyly. Interfamilial variations of published cases suggest subdivision of a new nosologic group.

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Year:  1982        PMID: 6279340     DOI: 10.1111/j.1399-0004.1982.tb02083.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Authors:  S E Palmer; S W Scherer; M Kukolich; E M Wijsman; L C Tsui; K Stephens; J P Evans
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

2.  A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs.

Authors:  R L Maas; L I Jepeal; S L Elfering; R F Holcombe; C C Morton; R L Eddy; M G Byers; T B Shows; P Leder
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

  2 in total

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