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- W2081301372 abstract "A mother with poorly controlled congenital hypoparathyroidism and her infant with intra-uterine hyperparathyroidism were described in a previous publication.1In that paper, the pathophysiology of the undermineralized bones of the infant was discussed. We have had the unusual opportunity to study a second child of this hypoparathyroid mother; this infant has congenital hypoparathyroidism. Since there are few data on the dose of vitamin D or parathyroid hormone in infants with congenital hypoparathyroidism, we are reporting our management of this newborn and particular success on treating her with weekly doses of ergocalciferol (vitamin D2) orally. As both infants were in a similar intrauterine environment, we have more information pertaining to the pathophysiology of the skeletal lesions seen in the first baby at birth. Report of a Case The patient was born to a gravida 2, para 1, 25-year-old mother untreated for congenital hypoparathyroidism, paranoid schizophrenia, epilepsy, and chronic pyelonephritis." @default.
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- W2081301372 date "1970-01-01" @default.
- W2081301372 modified "2023-09-27" @default.
- W2081301372 title "Congenital Familial Hypoparathyroidism" @default.
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- W2081301372 doi "https://doi.org/10.1001/archpedi.1970.02100050076018" @default.
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