| Literature DB >> 8275561 |
M Haim1.
Abstract
Genetic classification of retinitis pigmentosa (RP) can be problematic, due to a large number of isolated cases, reduced penetrance, and considerable variation in expressivity. Another confounder is a high proportion of affected female carriers in X-linked RP. Based on the genetic definitions of five different authors, a reclassification experiment was conducted with 350 Danish families. Agreement existed about a small "nucleus" of familial cases. Most definitions favored autosomal dominant inheritance at the expense of X-linked. The experiment revealed that methodological differences to a large extent might explain the considerable variation among reported genetic frequencies of retinitis pigmentosa.Entities:
Mesh:
Year: 1993 PMID: 8275561 DOI: 10.1111/j.1399-0004.1993.tb03848.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438