Literature DB >> 2063903

Generalized enchondromatosis in a boy with only platyspondyly in the father.

F Halal1, E M Azouz.   

Abstract

We report on a boy with platyspondyly and metaphyseal manifestations of enchondromatosis with severe involvement of hands and feet, compatible with generalized enchondromatosis (enchondromatosis Spranger type VI). His father has only moderate platyspondyly. The latter is either coincidental or a milder, more localized expression of the disease. Father and son have consanguineous parents suggesting autosomal recessive inheritance of the trait. However, autosomal dominant inheritance with variable expressivity is also possible.

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Year:  1991        PMID: 2063903     DOI: 10.1002/ajmg.1320380418

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


  9 in total

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2.  Dysmorphic facies and diffuse posterior spine ankylosis in a patient with unusual form of spondyloenchondrodysplasia (Spranger type IV).

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5.  Acroform type of enchondromatosis associated with severe vertebral involvement and facial dysmorphism in a boy with a new variant of enchondromatosis type I1 of Spranger: case report and a review of the literature.

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Review 7.  Ollier disease.

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9.  Spinal and extraspinal deformities in a patient with dysspondyloenchondromatosis.

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  9 in total

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