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Volumn 57, Issue 7, 2010, Pages 587-593

Etiology of congenital hypothyroidism using thyroglobulin and ultrasound combination

Author keywords

Congenital hypothyroidism; Scintigraphy; Thyroglobulin; Thyroid dysgenesis; Ultrasound

Indexed keywords

IODINE 131; LEVOTHYROXINE; PERTECHNETIC ACID TC 99M; SODIUM PERCHLORATE; THYROGLOBULIN; THYROTROPIN; THYROXINE;

EID: 77955821703     PISSN: 09188959     EISSN: 13484540     Source Type: Journal    
DOI: 10.1507/endocrj.K10E-009     Document Type: Article
Times cited : (21)

References (37)
  • 2
    • 18844376979 scopus 로고    scopus 로고
    • Hypothyroidism in Infants and Children
    • edn 9th, Eds Braverman LEUtiger RD. New York: Lippincott Williams & Wilkins
    • Vliet GV 2005 Hypothyroidism in Infants and Children. In The Thyroid - A Fundamental and Clinical Text, edn 9th, 1029-1032. Eds Braverman LEUtiger RD. New York: Lippincott Williams & Wilkins.
    • (2005) The Thyroid - a Fundamental and Clinical Text , pp. 1029-1032
    • Vliet, G.V.1
  • 3
    • 0041328169 scopus 로고    scopus 로고
    • An outline of inherited disorders of the thyroid hormone generating system
    • Knobel M, Medeiros-Neto G (2003) An outline of inherited disorders of the thyroid hormone generating system. Thyroid 13: 771-801.
    • (2003) Thyroid , vol.13 , pp. 771-801
    • Knobel, M.1    Medeiros-Neto, G.2
  • 4
    • 0036093069 scopus 로고    scopus 로고
    • Perspective: Genetic defects in the etiology of congenital hypothyroidism
    • Kopp P (2002) Perspective: genetic defects in the etiology of congenital hypothyroidism. Endocrinology 143: 2019-2024.
    • (2002) Endocrinology , vol.143 , pp. 2019-2024
    • Kopp, P.1
  • 5
    • 18844400822 scopus 로고    scopus 로고
    • Genetics of congenital hypothyroidism
    • Park SM, Chatterjee VK (2005) Genetics of congenital hypothyroidism. J Med Genet 42: 379-389.
    • (2005) J Med Genet , vol.42 , pp. 379-389
    • Park, S.M.1    Chatterjee, V.K.2
  • 6
    • 0024982280 scopus 로고
    • Molecular biology of the genetic defects of synthesis, transport and peripheral action of the thyroid gland hormones
    • Medeiros-Neto G (1990) Molecular biology of the genetic defects of synthesis, transport and peripheral action of the thyroid gland hormones. Rev Hosp Clin Fac Med Sao Paulo 45: 29-37.
    • (1990) Rev Hosp Clin Fac Med Sao Paulo , vol.45 , pp. 29-37
    • Medeiros-Neto, G.1
  • 11
    • 0041664888 scopus 로고    scopus 로고
    • Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hipothyroidism during L-thyroxine replacement
    • Fugazzola L (2003) Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hipothyroidism during L-thyroxine replacement. Clin Endocrinol 59: 230-236.
    • (2003) Clin Endocrinol , vol.59 , pp. 230-236
    • Fugazzola, L.1
  • 14
    • 33845257060 scopus 로고    scopus 로고
    • Combined ultrasound and isotope scanning is more informative in the diagnosis of congenital hypothyroidism than single scanning
    • Perry RJ, Maroo S, Maclennan AC, Jones JH, Donaldson MD (2006) Combined ultrasound and isotope scanning is more informative in the diagnosis of congenital hypothyroidism than single scanning. Arch Dis Child 91: 972-976.
    • (2006) Arch Dis Child , vol.91 , pp. 972-976
    • Perry, R.J.1    Maroo, S.2    Maclennan, A.C.3    Jones, J.H.4    Donaldson, M.D.5
  • 15
    • 0041324799 scopus 로고    scopus 로고
    • Accuracy of ultrasonography to establish the diagnosis and aetiology of permanent primary congenital hypothyroidism
    • Kreisner E, Camargo-Neto E, Maia CR, Gross JL (2003) Accuracy of ultrasonography to establish the diagnosis and aetiology of permanent primary congenital hypothyroidism. Clin Endocrinol (Oxf) 59: 361-365.
    • (2003) Clin Endocrinol (Oxf) , vol.59 , pp. 361-365
    • Kreisner, E.1    Camargo-Neto, E.2    Maia, C.R.3    Gross, J.L.4
  • 16
    • 0345305678 scopus 로고    scopus 로고
    • Color Doppler Ultrasonography: Diagnosis of Ectopic Thyroid Gland in Patients with Congenital Hypothyroidism Caused by Thyroid Dysgenesis
    • Ohnishi H, Sato H, Noda H, Inomata H, Sasaki N (2003) Color Doppler Ultrasonography: Diagnosis of Ectopic Thyroid Gland in Patients with Congenital Hypothyroidism Caused by Thyroid Dysgenesis. J Clin Endocrinol Metab 88: 5145-5149.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 5145-5149
    • Ohnishi, H.1    Sato, H.2    Noda, H.3    Inomata, H.4    Sasaki, N.5
  • 19
    • 0020647088 scopus 로고
    • Plasma thyroglobulin measurements help determine the type of thyroid defect in congenital hypothyroidism
    • Czernichow P, Schlumberger M, Pomarede R, Fragu P (1983) Plasma thyroglobulin measurements help determine the type of thyroid defect in congenital hypothyroidism. J Clin Endocrinol Metab 56: 242-245.
    • (1983) J Clin Endocrinol Metab , vol.56 , pp. 242-245
    • Czernichow, P.1    Schlumberger, M.2    Pomarede, R.3    Fragu, P.4
  • 20
    • 0028939561 scopus 로고
    • Measurement of thyroglobulin in newborn screening specimens from normal and hypothyroid infants
    • Mitchell ML, Hermos RJ (1995) Measurement of thyroglobulin in newborn screening specimens from normal and hypothyroid infants. Clin Endocrinol (Oxf) 42: 523-527.
    • (1995) Clin Endocrinol (Oxf) , vol.42 , pp. 523-527
    • Mitchell, M.L.1    Hermos, R.J.2
  • 21
    • 0023956326 scopus 로고
    • Thyroid scanning, ultrasound, and serum thyroglobulin in determining the origin of congenital hypothyroidism
    • Muir A, Daneman D, Daneman A, Ehrlich R (1988) Thyroid scanning, ultrasound, and serum thyroglobulin in determining the origin of congenital hypothyroidism. Am J Dis Child 142: 214-216.
    • (1988) Am J Dis Child , vol.142 , pp. 214-216
    • Muir, A.1    Daneman, D.2    Daneman, A.3    Ehrlich, R.4
  • 22
    • 4344632891 scopus 로고    scopus 로고
    • Twenty years later: A reevaluation of the contribution of plasma thyroglobulin to the diagnosis of thyroid dysgenesis in infants with congenital hypothyroidism
    • Djemli A, Fillion M, Belgoudi J, Lambert R, Delvin EE, Schneider W, Van Vliet G (2004) Twenty years later: a reevaluation of the contribution of plasma thyroglobulin to the diagnosis of thyroid dysgenesis in infants with congenital hypothyroidism. Clin Biochem 37: 818-822.
    • (2004) Clin Biochem , vol.37 , pp. 818-822
    • Djemli, A.1    Fillion, M.2    Belgoudi, J.3    Lambert, R.4    Delvin, E.E.5    Schneider, W.6    van Vliet, G.7
  • 24
    • 0025323524 scopus 로고
    • Normal volume of the thyroid gland in children
    • Ueda D (1990) Normal volume of the thyroid gland in children. J Clin Ultrasound 18: 455-462.
    • (1990) J Clin Ultrasound , vol.18 , pp. 455-462
    • Ueda, D.1
  • 26
    • 0030983833 scopus 로고    scopus 로고
    • Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism
    • Biebermann H, Schoneberg T, Krude H, Schultz G, Gudermann T, Gruters A (1997) Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism. J Clin Endocrinol Metab 82: 3471-3480.
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3471-3480
    • Biebermann, H.1    Schoneberg, T.2    Krude, H.3    Schultz, G.4    Gudermann, T.5    Gruters, A.6
  • 30
    • 0030481624 scopus 로고    scopus 로고
    • Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones
    • Medeiros-Neto G, Kim PS, Yoo SE, Vono J, Targovnik HM, Camargo R, Hossain SA, Arvan P (1996) Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones. J Clin Invest 98: 2838-2844.
    • (1996) J Clin Invest , vol.98 , pp. 2838-2844
    • Medeiros-Neto, G.1    Kim, P.S.2    Yoo, S.E.3    Vono, J.4    Targovnik, H.M.5    Camargo, R.6    Hossain, S.A.7    Arvan, P.8
  • 33
    • 13444292378 scopus 로고    scopus 로고
    • Pendred syndrome
    • discussion 204
    • Glaser B (2003) Pendred syndrome. Pediatr Endocrinol Rev 1 Suppl 2: 199-204; discussion 204.
    • (2003) Pediatr Endocrinol Rev , vol.1 , Issue.SUPPL. 2 , pp. 199-204
    • Glaser, B.1
  • 34
    • 0347993689 scopus 로고    scopus 로고
    • Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect
    • Nascimento AC, Guedes DR, Santos CS, Knobel M, Rubio IG, Medeiros-Neto G (2003) Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect. Thyroid 13: 1145-1151.
    • (2003) Thyroid , vol.13 , pp. 1145-1151
    • Nascimento, A.C.1    Guedes, D.R.2    Santos, C.S.3    Knobel, M.4    Rubio, I.G.5    Medeiros-Neto, G.6
  • 35
    • 16844375500 scopus 로고    scopus 로고
    • Children with congenital hypothyroidism and their siblings: Do they really differ?
    • Rovet JF (2005) Children with congenital hypothyroidism and their siblings: do they really differ? Pediatrics 115: e52-57.
    • (2005) Pediatrics , vol.115
    • Rovet, J.F.1
  • 36
    • 0035671831 scopus 로고    scopus 로고
    • The influence of etiology and treatment factors on intellectual outcome in congenital hypothyroidism
    • Song SI, Daneman D, Rovet J (2001) The influence of etiology and treatment factors on intellectual outcome in congenital hypothyroidism. J Dev Behav Pediatr 22: 376-384.
    • (2001) J Dev Behav Pediatr , vol.22 , pp. 376-384
    • Song, S.I.1    Daneman, D.2    Rovet, J.3
  • 37
    • 56649086658 scopus 로고    scopus 로고
    • Should the levothyroxine starting dose be tailored to disease severity in neonates with congenital hypothyroidism?
    • LaFranchi SH (2008) Should the levothyroxine starting dose be tailored to disease severity in neonates with congenital hypothyroidism? Nat Clin Pract Endocrinol Metab 4: 658-659.
    • (2008) Nat Clin Pract Endocrinol Metab , vol.4 , pp. 658-659
    • la Franchi, S.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.