Literature DB >> 1261071

Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardation.

G Neuhäuser, E G Kaveggia, J M Opitz.   

Abstract

We report a sibship of three sisters and two brothers who showed osteoporosis of variable severity; the propositus has incapacitating deformities following numerous fractures. Four of the sibs, including three with frequent fractures, were blind from infancy ("pseudogliomatous blindness"). In addition, two were mentally retarded. The osteoporosis-pseudoglioma syndrome is inherited as an autosomal recessive trait; similar reports from the literature support this assumption.

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Year:  1976        PMID: 1261071     DOI: 10.1111/j.1399-0004.1976.tb01581.x

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


  8 in total

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  8 in total

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