Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Indian J Ophthalmol ; 1996 Jun; 44(2): 77-82
Article in English | IMSEAR | ID: sea-70765

ABSTRACT

A total of 151 retinitis pigmentosa (RP) patients from 83 families were screened and the frequencies of different genetic categories studied. One hundred and ten patients out of 151 had a positive inheritance pattern, and autosomal recessive (AR) emerged as the predominant (53 out of 151), genetic pattern followed by isolated or sporadic (41 out of 151) cases. Further study of autosomal recessive cases revealed consanguinity as the main characteristic (49 out of 53) in the Indian population studied. Early onset and severe progression of disease was seen in the consanguineous group.


Subject(s)
Consanguinity , Disease Progression , Female , Humans , India/epidemiology , Male , Pedigree , Retinitis Pigmentosa/classification
SELECTION OF CITATIONS
SEARCH DETAIL