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  Vol. 131 No. 7, July 1977 TABLE OF CONTENTS
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Picture of the Month

Sydney S. Gellis, MD; Murray Feingold, MD; J. P. Farriaux, MD; G. Fontaine, MD

Am J Dis Child. 1977;131(7):807-808.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Denoument and Discussion

Pseudohypoparathyroidism

Manifestations

Manifestations are shortness of stature, obesity, rounded faces, shortening of one or more metacarpals and metatarsals, and mental retardation. Convulsions may occur, and calcifications are frequently present within the brain and in subcutaneous tissues. Not all end organs (kidney, bone, and intestine) are equally affected, and, therefore, there are several clinical forms of pseudohypoparathyroidism.

Biochemical findings of diagnostic importance are hypocalcemia and hyperphosphatemia that, unlike idiopathic hypoparathyroidism, remain uninfluenced by exogenous parathormone injection (Ellsworth-Howard test). The urinary excretion of cyclic adenosine monophosphate (AMP) is also not increased by parathormone injections. Serum parathormone levels are increased because of lack of the feedback regulatory influence by cyclic AMP.

It appears that pseudohypoparathyroidism and psuedo-psuedohypoparathyroidism are closely related. The latter is clinically similar to pseudohypoparathyroidism, but biochemical findings are different. Occurrences of normocalcemic and hypocalcemic patients within one family help support the hypothesis that both entities are similar. . . . [Full Text PDF of this Article]


Author Affiliations



From the Clinique Pediatrique, Cite Hospitaliere Regional de Lille, France.


Footnotes



Reprint requests to Boston Floating Hospital, 20 Ash St, Boston, MA 02111 (Dr Gellis).



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