Abstract
This chapter focuses on the rare disorder of hypoparathyroidism in children. It details the clinical features, pathophysiology, and biochemical abnormalities of the many forms seen clinically. Up-to-date information about the genetics of these disorders is provided along with the abnormalities in gene function. The chapter concludes with a summary of current treatment options for children with these disorders.
Author supplied keywords
- 1,25 Dihydroxy vitamin D
- APECED syndrome
- Acquired hypoparathyroidism
- Activating and inhibiting mutations
- Acute pancreatitis
- Alfacalcidol
- Aluminum hydroxide
- Antiepileptic drugs
- Autosomal dominant hypoparathyroidism
- Basal ganglia
- Behavioral problems
- Calcifications of basal ganglia
- Calcium chelators
- Calcium receptor antibodies
- Calcium sensing receptors
- Cardioversion disturbances
- Chemotherapy
- Chvostek sign
- Cleft palate
- Currently
- Cytochrome P450
- Deafness
- Deficiency of PTH production
- Dental hypoplasia
- DiGeorge syndrome
- Distal renal tubular reabsorption
- Dysmorphism
- Embryological development
- Exogenous PTH
- FARR syndrome
- Familial hypoparathyroidism X linked length recessive transmission
- Fluorescent in situ hybridization
- G protein coupled receptors
- Glial cell missing B transcription factor
- Heart is normal dominant hypocalcemia
- Hypertelorism
- Hypocalcemia
- Hypomagnesemia
- Hypoparathyroidism
- Iatrogenic causes of hypocalcemia
- Immunological disorders
- Increased urinary calcium excretion
- Infectious syndromes
- Invasive tumors
- Ionized calcium
- Kearns-Sayre syndrome
- Kenny-Caffey syndrome
- Ketoconazole
- Laryngospasm
- Laxatives
- Lithiasis
- Maternal hyperparathyroidism and neonatal hypoparathyroidism
- Mental retardation
- Metaphysis
- Microcephaly
- Micrognathia
- Mitochondrial disease
- Mutation in PTH gene
- NA LP 5 protein
- Nephrocalcinosis
- Neuromuscular irritability
- Osteosarcoma
- Parathyroid hormone
- Paresthesias
- Philtrum
- Phosphatemia
- Pseudo-Bartter syndrome
- Psychological manifestations
- Radiological signs
- Renal 1 alpha hydroxylase
- Renal dysplasia syndrome
- Retardation
- Rhabdomyolysis
- SOX3
- Sanjad-Sakati syndrome
- Seizures
- Septic shock
- Surgery
- TBX.1 gene
- Teriparatide
- Thymic aplasia
- Transcription factors
- Treatment
- Trousseau sign
- Urinary calcium
- Urogenital, skeletal, ocular malformations
Cite
CITATION STYLE
APA
Lienhardt-Roussie, A., & Linglart, A. (2012). Hypoparathyroidism in children. In Diseases of the Parathyroid Glands (Vol. 9781441955500, pp. 299–310). Springer New York. https://doi.org/10.1007/978-1-4419-5550-0_16
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free