Literature DB >> 8368255

Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.

L S Sadler1, L K Robinson.   

Abstract

Recently we evaluated an American family with the chorioretinal dysplasia-microcephaly-mental retardation syndrome (CDMMS, McKusick #156590). The male-to-male transmission observed for the first time in the family of this report confirms autosomal dominant inheritance. Analysis of our cases and review of the literature illustrates the variable expressivity of this disorder and demonstrates the need for careful ophthalmologic evaluations of at-risk relatives in order to provide accurate recurrence risks.

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Year:  1993        PMID: 8368255     DOI: 10.1002/ajmg.1320470114

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy.

Authors:  Maria F Shurygina; Joseph M Simonett; Maria A Parker; Amanda Mitchell; Florin Grigorian; Jacob Lifton; Aaron Nagiel; Alexander A Shpak; Elena L Dadali; Irina A Mishina; Richard G Weleber; Paul Yang; Mark E Pennesi
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-11-02       Impact factor: 4.799

  1 in total

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