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Volumn 9781441955500, Issue , 2012, Pages 299-310

Hypoparathyroidism in children

Author keywords

1,25 Dihydroxy vitamin D; Acquired hypoparathyroidism; Activating and inhibiting mutations; Acute pancreatitis; Alfacalcidol; Aluminum hydroxide; Antiepileptic drugs; APECED syndrome; 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; Familial hypoparathyroidism X linked length recessive transmission; FARR syndrome; 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; Sanjad Sakati syndrome; Seizures; Septic shock; SOX3; Surgery; TBX.1 gene; Teriparatide; Thymic aplasia; Transcription factors; Treatment; Trousseau sign; Urinary calcium; Urogenital, skeletal, ocular malformations

Indexed keywords


EID: 84927747207     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-1-4419-5550-0_16     Document Type: Chapter
Times cited : (3)

References (48)
  • 3
    • 0035005477 scopus 로고    scopus 로고
    • Gcm2 and foxn1 mark early parathyroid- and thymus-specifi c domains in the developing third pharyngeal pouch
    • Gordon J, Bennett AR, Blackburn CC, Manley NR. Gcm2 and Foxn1 mark early parathyroid- And thymus-specifi c domains in the developing third pharyngeal pouch. Mech Dev. 2001; 103: 141-3
    • (2001) Mech Dev , vol.103 , pp. 141-143
    • Gordon, J.1    Bennett, A.R.2    Blackburn, C.C.3    Manley, N.R.4
  • 4
    • 0036531911 scopus 로고    scopus 로고
    • Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission
    • Iascone MR, Vittorini S, Sacchelli M, Spadoni I, Simi P, Giusti S. Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission. Am J Med Genet. 2002; 108: 319-21
    • (2002) Am J Med Genet , vol.108 , pp. 319-321
    • Iascone, M.R.1    Vittorini, S.2    Sacchelli, M.3    Spadoni, I.4    Simi, P.5    Giusti, S.6
  • 8
    • 35348822545 scopus 로고    scopus 로고
    • Velocardiofacial syndrome digeorge syndrome: The chromosome 22q11.2 deletion syndromes
    • Kobrynski LJ, Sullivan KE. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet. 2007; 370: 1443-52
    • (2007) Lancet , vol.370 , pp. 1443-1452
    • Kobrynski, L.J.1    Sullivan, K.E.2
  • 10
    • 77952328830 scopus 로고    scopus 로고
    • Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome
    • Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol. 2010; 105: 1617-24
    • (2010) Am J Cardiol , vol.105 , pp. 1617-1624
    • Momma, K.1
  • 11
    • 44149113011 scopus 로고    scopus 로고
    • Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome
    • Prasad SE, Howley S, Murphy KC. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome. Dev Disabil Res Rev. 2008; 14: 26-34
    • (2008) Dev Disabil Res Rev , vol.14 , pp. 26-34
    • Prasad, S.E.1    Howley, S.2    Murphy, K.C.3
  • 12
    • 0034772381 scopus 로고    scopus 로고
    • Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor gcmb
    • Ding C, Buckingham B, Levine MA. Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB. J Clin Invest. 2001; 108: 1215-20
    • (2001) J Clin Invest , vol.108 , pp. 1215-1220
    • Ding, C.1    Buckingham, B.2    Levine, M.A.3
  • 15
    • 34247149887 scopus 로고    scopus 로고
    • Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia
    • Liu Z, Yu S, Manley NR. Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia. Dev Biol. 2007; 305: 333-46
    • (2007) Dev Biol , vol.305 , pp. 333-346
    • Liu, Z.1    Yu, S.2    Manley, N.R.3
  • 16
    • 10644230307 scopus 로고    scopus 로고
    • Gcmb gene, a master regulator of parathyroid gland development, expression, and regulation in hyperparathyroidism
    • Kebebew E, Peng M, Wong MG, Ginzinger D, Duh QY, Clark OH. GCMB gene, a master regulator of parathyroid gland development, expression, and regulation in hyperparathyroidism. Surgery. 2004; 136: 1261-6
    • (2004) Surgery , vol.136 , pp. 1261-1266
    • Kebebew, E.1    Peng, M.2    Wong, M.G.3    Ginzinger, D.4    Duh, Q.Y.5    Clark, O.H.6
  • 21
    • 33846952194 scopus 로고    scopus 로고
    • Parathyroid development and the role of tubulin chaperone e
    • Parvari R, Diaz GA, Hershkovitz E. Parathyroid development and the role of tubulin chaperone E. Horm Res. 2007; 67: 12-21
    • (2007) Horm Res , vol.67 , pp. 12-21
    • Parvari, R.1    Diaz, G.A.2    Hershkovitz, E.3
  • 25
    • 1442277000 scopus 로고    scopus 로고
    • Diseases associated with the extracellular calcium-sensing receptor
    • Thakker RV. Diseases associated with the extracellular calcium-sensing receptor. Cell Calcium. 2004; 35: 275-82
    • (2004) Cell Calcium , vol.35 , pp. 275-282
    • Thakker, R.V.1
  • 28
    • 64149091308 scopus 로고    scopus 로고
    • Thick ascending limb: The na(+): K (+): 2cl (-) co-Transporter, nkcc2, and the calcium-sensing receptor, casr
    • Gamba G, Friedman PA. Thick ascending limb: the Na(+): K (+): 2Cl (-) co-Transporter, NKCC2, and the calcium-sensing receptor, CaSR. Pfl ugers Arch. 2009; 458: 61-76
    • (2009) Pfl Ugers Arch , vol.458 , pp. 61-76
    • Gamba, G.1    Friedman, P.A.2
  • 30
    • 0022586447 scopus 로고
    • Familial isolated hypoparathyroidism: A molecular genetic analysis of 8 families with 23 affected persons
    • Ahn TG, Antonarakis SE, Kronenberg HM, Igarashi T, Levine MA. Familial isolated hypoparathyroidism: a molecular genetic analysis of 8 families with 23 affected persons. Medicine (Baltimore). 1986; 65: 73-81
    • (1986) Medicine (Baltimore , vol.65 , pp. 73-81
    • Ahn, T.G.1    Antonarakis, S.E.2    Kronenberg, H.M.3    Igarashi, T.4    Levine, M.A.5
  • 31
    • 0025013749 scopus 로고
    • Mutation of the signal peptideencoding region of the preproparathyroid hormone gene in familial isolated hypoparathyroidism
    • Arnold A, Horst SA, Gardella TJ, Baba H, Levine MA, Kronenberg HM. Mutation of the signal peptideencoding region of the preproparathyroid hormone gene in familial isolated hypoparathyroidism. J Clin Invest. 1990; 86: 1084-7
    • (1990) J Clin Invest , vol.86 , pp. 1084-1087
    • Arnold, A.1    Horst, S.A.2    Gardella, T.J.3    Baba, H.4    Levine, M.A.5    Kronenberg, H.M.6
  • 32
    • 0026547570 scopus 로고
    • The modulation of circulating parathyroid hormone immunoheterogeneity in man by ionized calcium concentration
    • D'Amour P, Palardy J, Bahsali G, Mallette LE, DeLean A, Lepage R The modulation of circulating parathyroid hormone immunoheterogeneity in man by ionized calcium concentration. J Clin Endocrinol Metab. 1992; 74: 525-32
    • (1992) J Clin Endocrinol Metab , vol.74 , pp. 525-532
    • D'amour, P.1    Palardy, J.2    Bahsali, G.3    Mallette, L.E.4    Delean, A.5    Lepage, R.6
  • 33
    • 0035001156 scopus 로고    scopus 로고
    • Severe hypomagnesemia and hypoparathyroidism in kearns-sayre syndrome
    • Katsanos KH, Elisaf M, Bairaktari E, Tsianos EV. Severe hypomagnesemia and hypoparathyroidism in Kearns-Sayre syndrome. Am J Nephrol. 2001; 21: 150-3
    • (2001) Am J Nephrol , vol.21 , pp. 150-153
    • Katsanos, K.H.1    Elisaf, M.2    Bairaktari, E.3    Tsianos, E.V.4
  • 34
    • 0343632387 scopus 로고    scopus 로고
    • Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial dna: A clinical and molecular genetic study of four children with kearns-sayre syndrome
    • Wilichowski E, Grüters A, Kruse K, Rating D, Beetz R, Korenke GC, Ernst BP, Christen HJ, Hanefeld F. Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome. Pediatr Res. 1997; 41: 193-200
    • (1997) Pediatr Res , vol.41 , pp. 193-200
    • Wilichowski, E.1    Grüters, A.2    Kruse, K.3    Rating, D.4    Beetz, R.5    Korenke, G.C.6    Ernst, B.P.7    Christen, H.J.8    Hanefeld, F.9
  • 35
    • 62749116015 scopus 로고    scopus 로고
    • Anti-parathyroid and anti-calcium sensing receptor antibodies in autoimmune hypoparathyroidism
    • x
    • Brown EM. Anti-parathyroid and anti-calcium sensing receptor antibodies in autoimmune hypoparathyroidism. Endocrinol Metab Clin N Am. 2009; 38: 437-45. x.
    • (2009) Endocrinol Metab Clin N Am , vol.38 , pp. 437-445
    • Brown, E.M.1
  • 41
    • 34249720917 scopus 로고    scopus 로고
    • Parathyroid risk in total thyroidectomy for bilateral, benign, multinodular goitre: Report of 351 surgical cases
    • Page C, Strunski V. Parathyroid risk in total thyroidectomy for bilateral, benign, multinodular goitre: report of 351 surgical cases. J Laryngol Otol. 2007; 121: 237-41
    • (2007) J Laryngol Otol , vol.121 , pp. 237-241
    • Page, C.1    Strunski, V.2
  • 43
    • 0025351821 scopus 로고
    • Nephrocalcinosis, hypercalciuria and elevated serum levels of 1,25-dihydroxyvitamin d in children possible link to vitamin d toxicity
    • Misselwitz J, Hesse V, Markestad T. Nephrocalcinosis, hypercalciuria and elevated serum levels of 1,25-dihydroxyvitamin D in children. Possible link to vitamin D toxicity. Acta Paediatr Scand. 1990; 79: 637-43
    • (1990) Acta Paediatr Scand , vol.79 , pp. 637-643
    • Misselwitz, J.1    Hesse, V.2    Markestad, T.3
  • 44
    • 0024153686 scopus 로고
    • Nephrocalcinosis in children and adolescents: Sonographic evaluation during long-Term treatment with 1,25-dihydroxycholecalciferol
    • Weber G, Cazzuffi MA, Frisone F, de Angelis M, Pasolini D, Tomaselli V, Chiumello G. Nephrocalcinosis in children and adolescents: sonographic evaluation during long-Term treatment with 1,25-dihydroxycholecalciferol. Child Nephrol Urol. 1988; 9: 273-6
    • (1988) Child Nephrol Urol , vol.9 , pp. 273-276
    • Weber, G.1    Cazzuffi, M.A.2    Frisone, F.3    De Angelis, M.4    Pasolini, D.5    Tomaselli, V.6    Chiumello, G.7
  • 45
    • 51649100312 scopus 로고    scopus 로고
    • Effects of once versus twice-daily parathyroid hormone 1-34 therapy in children with hypoparathyroidism
    • Winer KK, Sinaii N, Peterson D, Sainz B, Cutler GB. Effects of once versus twice-daily parathyroid hormone 1-34 therapy in children with hypoparathyroidism. J Clin Endocrinol Metab. 2008; 93: 3389-95
    • (2008) J Clin Endocrinol Metab , vol.93 , pp. 3389-3395
    • Winer, K.K.1    Sinaii, N.2    Peterson, D.3    Sainz, B.4    Cutler, G.B.5
  • 46
    • 80655148327 scopus 로고    scopus 로고
    • Long-Term results of continuous subcutaneous recombinant pth 1-34) infusion in children with refractory hypoparathyroidism
    • Linglart A, Rothenbuhler A, Gueorgieva I, Lucchini P, Silve C, Bougnères P. Long-Term results of continuous subcutaneous recombinant PTH (1-34) infusion in children with refractory hypoparathyroidism. J Clin Endocrinol Metab. 2011; 96(11): 3308-12
    • (2011) J Clin Endocrinol Metab , vol.96 , Issue.11 , pp. 3308-3312
    • Linglart, A.1    Rothenbuhler, A.2    Gueorgieva, I.3    Lucchini, P.4    Silve, C.5    Bougnères, P.6


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