Literature DB >> 29168277

Congenital limb deficiencies and major associated anomalies in Alberta for the years 1980-2012.

Tanya Bedard1, R Brian Lowry1,2,3, Barbara Sibbald1, Susan Crawford4, Gerhard N Kiefer1,5.   

Abstract

There is a wide range of the proportion of congenital anomalies associated with limb deficiencies reported in the literature. This variation is primarily attributed to methodology and classification differences. The distribution of associated anomalies among cases with congenital limb deficiencies in Alberta born between January 1, 1980 and December 31, 2012 is described. Of the 170 cases identified, most were live born (75.3%), male (61.8%), had longitudinal limb deficiencies (78.8%), and had associated anomalies outside the musculoskeletal system (77.6%). Significant associations between the preaxial longitudinal group and the central nervous, gastrointestinal, and cardiovascular systems are reported as well as between the postaxial longitudinal group and congenital hip and foot anomalies. Probable and possible syndrome diagnoses are described for cases with recognized malformation patterns.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  associated major congenital anomalies; congenital limb deficiency; etiology

Mesh:

Year:  2017        PMID: 29168277     DOI: 10.1002/ajmg.a.38513

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Support, information, and integration of genetics for children with congenital lower limb deficiencies in British Columbia, Canada.

Authors:  Teresa Campbell; Ching-Yi Jenny Chen; Harpreet Chhina; Rajpreet Chahal; Anthony Cooper; Alison M Elliott
Journal:  Paediatr Child Health       Date:  2019-02-12       Impact factor: 2.253

2.  Etiological diagnosis in limb reduction defects and the number of affected limbs: A population-based study in the Northern Netherlands.

Authors:  Jorieke E H Bergman; Katharina Löhner; Corry K van der Sluis; Patrick Rump; Hermien E K de Walle
Journal:  Am J Med Genet A       Date:  2020-09-21       Impact factor: 2.802

  2 in total

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