Literature DB >> 7296946

An Indian family with postaxial polydactyly in four generations.

K Kucheria, R K Kenue, N Taneja.   

Abstract

An Indian family was observed with postaxial polycactyly in four generations. Of the twelve affected cases, eleven were male and one was female. The affected males showed postaxial polydactyly Type A in both hands and feet. The affected female showed polysyndactyly and both Types A and B postaxial polydactyly. Study of this family strongly suggests a common causal factor for postaxial polydactyly Types A and B and polysyndactyly. The observations also support an autosomal dominant pattern of inheritance and a high degree of genetic heterogeneity in ths malformation.

Entities:  

Mesh:

Year:  1981        PMID: 7296946     DOI: 10.1111/j.1399-0004.1981.tb01803.x

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


  4 in total

1.  Sporadic familial ulnar hexadactyly of all four limbs.

Authors:  Uwe Wollina; Shyam B Verma
Journal:  J Dermatol Case Rep       Date:  2010-04-11

2.  Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Authors:  U Radhakrishna; J L Blouin; H Mehenni; U C Patel; M N Patel; J V Solanki; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

3.  The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.

Authors:  U Radhakrishna; D Bornholdt; H S Scott; U C Patel; C Rossier; H Engel; A Bottani; D Chandal; J L Blouin; J V Solanki; K H Grzeschik; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

4.  Clinical Genetics of Polydactyly: An Updated Review.

Authors:  Muhammad Umair; Farooq Ahmad; Muhammad Bilal; Wasim Ahmad; Majid Alfadhel
Journal:  Front Genet       Date:  2018-11-06       Impact factor: 4.599

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.