Abstract
Hypocalcemia in infants and adolescents can present with mild or severe symptoms involving the nervous, cardiovascular, and/or skeletal systems. The hallmark manifestation is neuromuscular excitability with tetany, muscle spasm, and/or seizure, though mild hypocalcemia may be asymptomatic. The causes of hypocalcemia may be transient or permanent, and include genetic, autoimmune, nutritional, acquired, and iatrogenic etiologies. A focused history, thorough physical examination, and key laboratory studies are essential steps in the diagnostic pathways and help direct further evaluation and management.
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Abbreviations
- AD:
-
Autosomal dominant
- ADH:
-
Autosomal dominant hypocalcemia
- AHO:
-
Albright’s hereditary osteodystrophy
- AIRE:
-
Autoimmune regulator
- APECED:
-
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
- AR:
-
Autosomal recessive
- cAMP:
-
Cyclic adenosine monophosphate
- CaSR:
-
Calcium-sensing receptor
- CHD7:
-
Chromodomain helicase DNAbinding 7
- EEG:
-
Electroencephalogram
- EKG:
-
Electrocardiogram
- FGF23:
-
Fibroblast growth factor 23
- GATA3:
-
GATA-binding factor 3
- GCM2:
-
Glial cell missing homologue 2
- GNAS:
-
Guanine nucleotide–binding protein alpha subunit
- HDR:
-
Hypoparathyroidism, sensorineural deafness, and renal disease
- HVDRR:
-
Hereditary vitamin D–resistant rickets
- MELAS:
-
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes
- MTP:
-
Mitochondrial trifunctional protein
- PHP:
-
Pseudohypoparathyroidism
- PTH:
-
Parathyroid hormone
- RANK:
-
Receptor activator of nuclear factor kappa-B ligand
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Vakharia, J.D., Topor, L.S. (2021). Hypocalcemia. In: Stanley, T., Misra, M. (eds) Endocrine Conditions in Pediatrics. Springer, Cham. https://doi.org/10.1007/978-3-030-52215-5_5
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