A Case of Renal Rickets Simulating "Metaphysial Dysostosis"

Müller, G; Sissons, H. A.

doi:10.1302/0301-620x.33b2.231

The Journal of Bone and Joint Surgery. British volume

1951

DOI: 10.1302/0301-620x.33b2.231

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A Case of Renal Rickets Simulating "Metaphysial Dysostosis"

G Müller

H. A. Sissons

Abstract: A case is described in which a clinical diagnosis of "metaphysial dysostosis" was made, but in which histological examination of involved bones showed the changes of rickets, presumably renal, with secondary hyperparathyroidism.

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1957

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Cited by 7 publications

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Metaphyseal Dysostosis Resembling Vitamin D-Refractory Rickets

Evans¹

1958

Arch Pediatr Adolesc Med

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The purpose of this paper is to describe a patient with an unclassified disorder of the metaphyses which, because of clinical, radiographic, and microscopic similarity to vitamin D-refractory rickets, was treated with toxic quantities of vitamin D. The resemblance of the metaphyseal lesions in the present case to the rare condition "metaphyseal dysostosis," described in 1934 by Murk Jansen, is discussed.

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Metaphyseal Dysostosis Resembling Vitamin D-Refractory Rickets

Evans¹

1958

Arch Pediatr Adolesc Med

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Metaphyseal chondrodysplasia, Schmid type Clinical and radiographic deliniation with a review of the literature

1988

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Analysis of 20 cases of metaphyseal chondrodysplasia, Schmid type as well as a review of the world literature reveals a specific autosomal dominant disorder that was often over-diagnosed in the past, sometimes resulting in incorrect genetic counselling. Significant radiologic features include an enlarged capital femoral epiphysis in early childhood, coxa vara, greater involvement of the distal femoral metaphysis than the proximal, anterior rib changes and a normal spine. Chondroosseous morphology is not specific. Presentation in nonfamilial cases is no earlier than the second year of life.

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Hypophosphatasia

Fraser¹

1957

The American Journal of Medicine

376

180

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A Case of Renal Rickets Simulating "Metaphysial Dysostosis"

Abstract: A case is described in which a clinical diagnosis of "metaphysial dysostosis" was made, but in which histological examination of involved bones showed the changes of rickets, presumably renal, with secondary hyperparathyroidism.

Cited by 7 publications

References 0 publications

Metaphyseal Dysostosis Resembling Vitamin D-Refractory Rickets

Metaphyseal Dysostosis Resembling Vitamin D-Refractory Rickets

Metaphyseal chondrodysplasia, Schmid type Clinical and radiographic deliniation with a review of the literature

Hypophosphatasia

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