Pseudo‐Pseudohypoparathyroidism A Report of two Cases

SUMMARYA large kindred (4 generations) with pseudo-pseudo-hypoparathyroidism (PPHP) and the clinical, biological and anthropometric features of this syndrome are extensively described.The association of PPHP with diabetes, hypertension, hypothyroidism, polyarthrosis and peripheral arteritis is very probably significant.Gonadal dysgenesis with brachymetacarpy must clearly be distinguished from PPHP.The transmission of PPHP is probably not sex-linked dominant but autosomal dominant with an incomplete penetrance of about 50%, a varying expressivity and weak familial specificity. Partial sex limiting or sex predominance may occur, instead of true sex-linkage in this condition.

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Mineralization of the central nervous system in pseudopseudohypoparathyroidism (PPH).

Dudley¹,

Hawkins²

1970

Journal of Neurology, Neurosurgery & Psychiatry

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Pseudo‐Pseudohypoparathyroidism A Report of two Cases

Cited by 3 publications

References 17 publications

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Albright's Hereditary Poly-Osteochondrodystrophy — (Pseudo-pseudo-hypoparathyroidism with diabetes hypertension, arteritis and polyarthrosis)

Mineralization of the central nervous system in pseudopseudohypoparathyroidism (PPH).

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