Literature DB >> 437795

Inheritance of Indian childhood cirrhosis.

S S Agarwal, U C Lahori, S K Mehta, D G Smith, P C Bajpai.   

Abstract

Detailed pedigree charts were prepared from 120 index patients suffering from Indian childhood cirrhosis (ICC). Of the 120 families, 84 were informative for segregation analysis. Since families were ascertained through patients who came to hospital for treatment, the data were analyzed according to a single-selection model. The observed segregation ratio for the entire data was significantly lower than the one expected under the hypothesis of autosomal recessive inheritance (p = smaller than 0.005). On the other hand, the segregation data for families with at least two affected children (multiplex families) were compatible with autosomal recessive inheritance. On this basis, however, at least 50% of all the cases of ICC would have to be of nongenetic origin. Alternatively, analysis of the data by the Falconer method indicated that ICC could be of multifactorial origin with very strong genetic determination (over 85%).

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Year:  1979        PMID: 437795     DOI: 10.1159/000153021

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  3 in total

1.  hCTR1: a human gene for copper uptake identified by complementation in yeast.

Authors:  B Zhou; J Gitschier
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

2.  Indian childhood cirrhosis.

Authors:  M S Tanner; B Portmann
Journal:  Arch Dis Child       Date:  1981-01       Impact factor: 3.791

3.  Liver disease in India.

Authors:  S A Bhave; A N Pandit; A M Pradhan; D G Sidhaye; A Kantarjian; A Williams; I C Talbot; M S Tanner
Journal:  Arch Dis Child       Date:  1982-12       Impact factor: 3.791

  3 in total

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