Pre-adolescent resistant rickets in the African - a probable new syndrome

R. Bullock; M. Gelfand

Pre-adolescent resistant rickets in the African - a probable new syndrome

R. Bullock, M. Gelfand

Neurological Surgery

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Eleven cases of Vitamin D resistant rickets are reviewed. Diagnostic criteria and guidelines for management are discussed. Features of significance in this small series were the relatively large number of adult onset hypophosphataemia cases, in the face of their acknowledged rarity, and the absence of cases of Fanconi syndrome or renal tubular acidosis. Two of the cases showing the features of hypophosphataemic osteomalacia had a severe form of bilharzial uropathy.

Original language	English (US)
Pages (from-to)	217-227
Number of pages	11
Journal	Central African Journal of Medicine
Volume	23
Issue number	10
State	Published - Dec 1 1977

ASJC Scopus subject areas

Medicine(all)

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title = "Pre-adolescent resistant rickets in the African - a probable new syndrome",

abstract = "Eleven cases of Vitamin D resistant rickets are reviewed. Diagnostic criteria and guidelines for management are discussed. Features of significance in this small series were the relatively large number of adult onset hypophosphataemia cases, in the face of their acknowledged rarity, and the absence of cases of Fanconi syndrome or renal tubular acidosis. Two of the cases showing the features of hypophosphataemic osteomalacia had a severe form of bilharzial uropathy.",

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AU - Gelfand, M.

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N2 - Eleven cases of Vitamin D resistant rickets are reviewed. Diagnostic criteria and guidelines for management are discussed. Features of significance in this small series were the relatively large number of adult onset hypophosphataemia cases, in the face of their acknowledged rarity, and the absence of cases of Fanconi syndrome or renal tubular acidosis. Two of the cases showing the features of hypophosphataemic osteomalacia had a severe form of bilharzial uropathy.

AB - Eleven cases of Vitamin D resistant rickets are reviewed. Diagnostic criteria and guidelines for management are discussed. Features of significance in this small series were the relatively large number of adult onset hypophosphataemia cases, in the face of their acknowledged rarity, and the absence of cases of Fanconi syndrome or renal tubular acidosis. Two of the cases showing the features of hypophosphataemic osteomalacia had a severe form of bilharzial uropathy.

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M3 - Article

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Pre-adolescent resistant rickets in the African - a probable new syndrome

Abstract

ASJC Scopus subject areas

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