Literature DB >> 1858724

Partial hypoparathyroidism. A variant of transient congenital hypoparathyroidism.

S W Kooh1, A Binet.   

Abstract

We encountered three children who had neonatal hypocalcemia followed by a period of normocalcemia and recurrence of hypocalcemia later in childhood. They were full-term infants with normal birth weights who developed hypocalcemia within the first 48 hours after birth. The hypocalcemia resolved in 1 week, 3 months, and 14 months in the three patients. The recurrences of hypocalcemia occurred at 4, 7, and 12 years of age. Their plasma parathyroid hormone concentrations were consistently low but detectable. We suggest that partial hypoparathyroidism is the underlying abnormality in these patients and that neonatal hypocalcemia in otherwise healthy infants indicates the need for calcium measurements during childhood and adolescence.

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Year:  1991        PMID: 1858724     DOI: 10.1001/archpedi.1991.02160080053020

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  1 in total

1.  Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.

Authors:  Han-Yi Lin; Wen-Yu Tsai; Yi-Ching Tung; Shih-Yao Liu; Ni-Chung Lee; Yin-Hsiu Chien; Wuh-Liang Hwu; Cheng-Ting Lee
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-31       Impact factor: 5.555

  1 in total

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