Childhood Hypocalcemia: The Aetiological Pattern
Keywords:
aetiology, childhood, hypocalcemia
Abstract
Background: Hypocalcemia is not that rare condition and could be a potentially life threatening. Identifying the etiology is important for successful management. Design and setting: A retrospective, hospital based study was conducted at King Khalid University Hospital (KKUH), Riyadh, Saudi Arabia during the period December 1989 and June 2016. Materials and Methods: Medical records of children beyond the neonatal period with hypocalcemia were reviewed for aetiological diagnosis. Detailed history, clinical manifestation, and results of all the laboratory, and radiological investigations were obtained. Results: A total of 60 patients were seen in the period under review, December 1989 and June 2016, with childhood hypocalcemia. Twenty-seven (45.0%) patients were parathyroid hormone deficient, while rickets diagnosed in 25 (41.7%) patients. Conclusion: This study showed that parathyroid hormone (PTH) deficiency (45%) and rickets (41.7%) were the most common causes of childhood hypocalcemia.
Downloads
- Article PDF
- TEI XML Kaleidoscope (download in zip)* (Beta by AI)
- Lens* NISO JATS XML (Beta by AI)
- HTML Kaleidoscope* (Beta by AI)
- DBK XML Kaleidoscope (download in zip)* (Beta by AI)
- LaTeX pdf Kaleidoscope* (Beta by AI)
- EPUB Kaleidoscope* (Beta by AI)
- MD Kaleidoscope* (Beta by AI)
- FO Kaleidoscope* (Beta by AI)
- BIB Kaleidoscope* (Beta by AI)
- LaTeX Kaleidoscope* (Beta by AI)
How to Cite
References
R. Thakker (2003) Thakker RV; Parathyroid disorders and diseases altering calcium metabolism. 1851-1868. https://doi.org/10.1093/med/9780199204854.003.1306
J. Pettifor (2006) ed. Nutritional and induced rickets and osteomalacia: Primer on the metabolic and bone disorders and disorders of bone metabolism. 5th ed. 330-338.
Wharton B, Bishop N (2003) Rickets. 362, 1389-140.
Holick MF (2007) Vitamin D deficiency. 357, 266-81.
J. Eur (2015) Al Jurayyan NAM, Osman HA,; The increased prevalence of Congenital adrenal hyperplasia: The roles of consanguinity and multiple siblings involvement. 3(1), 31-34.
S. Saedi-Wong, A. Al-Frayh, H. Wong (1989) Socio - economic epidemiology of consanguineous mating's in Saudi Arabian population. 24, 247-252.
Shoback D (2008) Clinical practice, hypoparathyroidism. 359, 391-403.
Marx SJ (2000) Hypoparathyroidism and hyperperithyrodism disorders. 343, 1863-75.
Al Ali, A., Al Ayed, O., Al IssaSD, A. AlJurayyan, N. AL Jurayyan (2015) Al Ali AO, Al Ayed OA, Al IssaSD,AlJurayyan AN, AL Jurayyan NA; Autoimmune polyendocrine Syndrome type I, Int J recent Sci Res 2015. 6(7), 5058-5061.
S. Sanjad, N. Sakati, Y. Abu-Osba, R. Kaddoura, R. Milner (1991) A new Syndrome of Congenital hypoparathyroidism, severe growth failure and dysmorphicfeatures. 66, 193-196.
Anast CS, Winnacker JL, Forte LR, Burns TW Impaired release of parathyroid hormone in magnesium deficiency.
Published
2016-07-04
Issue
Section
License
Copyright (c) 2016 Authors and Global Journals Private Limited

This work is licensed under a Creative Commons Attribution 4.0 International License.