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Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism
Author(s) -
Korkmaz Hüseyin Anıl,
Özkan Behzat,
Terek Demet,
Ceyhun Dizdarer,
A. Sertac
Publication year - 2013
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.1037
Subject(s) - medicine , asymptomatic , hyperparathyroidism , pediatrics , vitamin d deficiency , fetus , epilepsy , pregnancy , vitamin d and neurology , endocrinology , psychiatry , biology , genetics
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 hyperparathyroidism and vitamin D deficiency. Physicians should be aware that undiagnosed maternal hyperparathyroidism can cause severe hypocalcemia in the newborn.

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