Neonatal hypocalcemia due to asymptomatic maternal primary hyperparathyroidism.
نویسندگان
چکیده
Neonatal hypocalcemia resulting from maternal primary hyperparathyroidism (MPH) is usually detected clinically in the first 2 weeks of life. Occasionally, diagnosis of primary hyperparathyroidism in a young asymptomatic mother is made when the infant presents with hypocalcemia. We present an infant with late onset hypocalcemia resulting from a combination of transient hypoparathyroidism due to asymptomatic MPH and vitamin D deficiency.
منابع مشابه
Late neonatal hypocalcemic tetany as a manifestation of unrecognized maternal primary hyperparathyroidism.
Maternal primary hyperparathyroidism causing hypercalcemia during pregnancy can suppress fetal and neonatal parathyroid hormone secretion. We report a newborn with transient hypoparathyroidism presented by hypocalcemic seizure and tetany on the 21st postnatal day in whom the final diagnosis was asymptomatic maternal primary hyperparathyroidism. Neonatal hypocalcemia usually occurs early in life...
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Maternal hypercalcemia suppresses parathyroid activity in the fetus resulting in impaired parathyroid responsiveness to hypocalcemia after birth. Resultant hypocalcemia may be severe and prolonged and rarely may lead to convulsions. Here, we present a newborn infant admitted to the pediatric emergency department at age two weeks with recurrent tonic convulsions due to asymptomatic maternal hype...
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A 32-day-old male infant had hypocalcaemic convulsions associated with asymptomatic maternal hyperparathyroidism. Very low total and ionised serum calcium, increased serum phosphate, and normal serum parathyroid hormone (PTH) and 25-hydroxycholecalciferol (25-OHD3) concentrations were found at admission. After treatment with calcium and vitamin D, serum PTH and 25-OHD3 concentrations increased ...
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ورودعنوان ژورنال:
- Indian pediatrics
دوره 42 3 شماره
صفحات -
تاریخ انتشار 2005