메뉴 건너뛰기




Volumn 48, Issue 2, 1997, Pages 83-87

Pubertal changes in testicular 3β-hydroxysteroid dehydrogenase activity in a male with classical 3β-hydroxysteroid dehydrogenase deficiency showing spontaneous secondary sexual maturation

Author keywords

3 Hydroxysteroid dehydrogenase deficiency; Congenital adrenal hyperplasia

Indexed keywords

GONADOTROPIN; HYDROXYSTEROID DEHYDROGENASE; STEROID; TESTOSTERONE;

EID: 0030757513     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000185492     Document Type: Article
Times cited : (13)

References (20)
  • 1
    • 0001763647 scopus 로고
    • The adrenogenital syndrome with deficiency of.Jp-hydroxystcroid dehydrogenase
    • Bongiovanni AM: The adrenogenital syndrome with deficiency of.Jp-hydroxystcroid dehydrogenase. J Clin Invest 1962:41:2086-2092.
    • (1962) J Clin Invest , vol.41 , pp. 2086-2092
    • Bongiovanni, A.M.1
  • 2
    • 0022650972 scopus 로고
    • Purification and characterization of rat adrenal 3p-hydroxysteroid dehydrogenase with steroid 5-ene-4-cne-isomerase
    • Ishii-Ohba H, Saiki N, Inano H, Tamaoki B: Purification and characterization of rat adrenal 3p-hydroxysteroid dehydrogenase with steroid 5-ene-4-cne-isomerase. J Steroid Biochem 1986:24:753-760.
    • (1986) J Steroid Biochem , vol.24 , pp. 753-760
    • Ishii-Ohba, H.1    Saiki, N.2    Inano, H.3    Tamaoki, B.4
  • 7
    • 0027971610 scopus 로고
    • Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3P-hydroxystcroid dehydrogenase deficiency
    • Rheaume E, Sanchez R, Simard J, Chang YT, Wang J, Pang S, Labrie F: Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3P-hydroxystcroid dehydrogenase deficiency. J Clin Endocrinol Mctab 1994:79:1012-1018.
    • (1994) J Clin Endocrinol Mctab , vol.79 , pp. 1012-1018
    • Rheaume, E.1    Sanchez, R.2    Simard, J.3    Chang, Y.T.4    Wang, J.5    Pang, S.6    Labrie, F.7
  • 8
    • 0028328226 scopus 로고
    • Detection and functional characterization of the novel mis-sense mutation Y254D in type II 3p-hydroxy-steroid dehydrogenase (3P-HSD) gene of a female patient with nonsalt-losing 3p-FISD deficiency
    • Sanchez R, Rheaume E, Laflamme N, Rosen-ficld R, Labrie F, Simard J: Detection and functional characterization of the novel mis-sense mutation Y254D in type II 3p-hydroxy-steroid dehydrogenase (3P-HSD) gene of a female patient with nonsalt-losing 3p-FISD deficiency. J Clin Endocrinol Metab 1994:78:561-567.
    • (1994) J Clin Endocrinol Metab , vol.78 , pp. 561-567
    • Sanchez, R.1    Rheaume, E.2    Laflamme, N.3    Rosen-Ficld, R.4    Labrie, F.5    Simard, J.6
  • 10
    • 0016187795 scopus 로고
    • Testicular endocrine function in a pubertal boy with 3p-hydroxystcroid dehydrogenase deficiency
    • Janne O, Perhcentupa J, Viinikka L, Vihko R: Testicular endocrine function in a pubertal boy with 3p-hydroxystcroid dehydrogenase deficiency. J Clin Endocrinol Mctab 1974:39:206-209.
    • (1974) J Clin Endocrinol Mctab , vol.39 , pp. 206-209
    • Janne, O.1    Perhcentupa, J.2    Viinikka, L.3    Vihko, R.4
  • 13
    • 0015149819 scopus 로고
    • Partial 3p-hydroxysteroid dehydrogenase (3P-HSD) deficiency in a family with congenital adrenal hyperplasia: Evidence for increasing 3p-HSD activity with age
    • Kenny FM, Reynolds JW, Green OC: Partial 3p-hydroxysteroid dehydrogenase (3P-HSD) deficiency in a family with congenital adrenal hyperplasia: Evidence for increasing 3p-HSD activity with age. Pediatrics 1971;48:756-765.
    • (1971) Pediatrics , vol.48 , pp. 756-765
    • Kenny, F.M.1    Reynolds, J.W.2    Green, O.C.3
  • 14
    • 0005133919 scopus 로고
    • Case of salt-losing congenital adrenal hyperplasia due to 3[J-hydroxvsteroid dehydrogenase deficiency: The first Japanese patient
    • Yoshimoto M, Baba T, Yokoo T, Matsumoto T, Hayashi S, Yasui M, Fukuda S, Yanagi T, Tsuji Y: Case of salt-losing congenital adrenal hyperplasia due to 3[J-hydroxvsteroid dehydrogenase deficiency: The first Japanese patient. Acta Paediatr J pn 1988:92:1964-1970.
    • (1988) Acta Paediatr J Pn , vol.92 , pp. 1964-1970
    • Yoshimoto, M.1    Baba, T.2    Yokoo, T.3    Matsumoto, T.4    Hayashi, S.5    Yasui, M.6    Fukuda, S.7    Yanagi, T.8    Tsuji, Y.9
  • 15
    • 0001837528 scopus 로고
    • Immunolocalization of 3($-hydroxystcroid dehydrogenase in human adrenal cortex and in its disorders
    • Sasatto H, Mason JI, Sasano N, Nagaura H: Immunolocalization of 3$-hydroxystcroid dehydrogenase in human adrenal cortex and in its disorders. F.ndocr Pathol Update 1990:1:94-101.
    • (1990) F.Ndocr Pathol Update , vol.1 , pp. 94-101
    • Sasatto, H.1    Mason, J.I.2    Sasano, N.3    Nagaura, H.4
  • 16
    • 0028002466 scopus 로고
    • Functional pathology of human ovarian steroidogenesis: Normal cycling ovary and steroid-producing neoplasma
    • Sasano H: Functional pathology of human ovarian steroidogenesis: Normal cycling ovary and steroid-producing neoplasma. Endocr Pathol Update 1994;5:81-89.
    • (1994) Endocr Pathol Update , vol.5 , pp. 81-89
    • Sasano, H.1
  • 17
    • 0024242392 scopus 로고
    • Human placental 3p-hydroxy-5-ene steroid dehydrogenase and steroid 5-4-ene-isomerase: Purification from microsomc. Substrate kinetics and inhibition by product steroids
    • Thomas JL, Berko EA, Faustino A, Mayers RP, Strieker RC: Human placental 3p-hydroxy-5-ene steroid dehydrogenase and steroid 5-4-ene-isomerase: Purification from microsomc. substrate kinetics and inhibition by product steroids. J Steroid Biochcm 1988;21:785-793.
    • (1988) J Steroid Biochcm , vol.21 , pp. 785-793
    • Thomas, J.L.1    Berko, E.A.2    Faustino, A.3    Mayers, R.P.4    Strieker, R.C.5
  • 18
    • 0029069535 scopus 로고
    • Molecular analysis of type II 3p-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3fl-hydroxysteroid dehydrogenase deficiency
    • Tajima T, Fujieda K, Nakae J, Shinohara N, Yoshimoto M, Baba T, Kinoshita E, lgarashi Y, Ohmura T: Molecular analysis of type II 3p-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3fl-hydroxysteroid dehydrogenase deficiency. Hum Mol Genet 1995:4:969-971.
    • (1995) Hum Mol Genet , vol.4 , pp. 969-971
    • Tajima, T.1    Fujieda, K.2    Nakae, J.3    Shinohara, N.4    Yoshimoto, M.5    Baba, T.6    Kinoshita, E.7    Lgarashi, Y.8    Ohmura, T.9
  • 19
    • 0014802807 scopus 로고
    • Unusual type of congenital adrenal hyperplasia probably due to deficiency of 3P-hydroxysteroid dehydrogenase. Case report of a surviving girl and steroid studies
    • Zachmann M, Vollmin JA, Murset G, Curtius H, Prader A: Unusual type of congenital adrenal hyperplasia probably due to deficiency of 3P-hydroxysteroid dehydrogenase. Case report of a surviving girl and steroid studies. J Clin Endocrinol 1970;30:719-726.
    • (1970) J Clin Endocrinol , vol.30 , pp. 719-726
    • Zachmann, M.1    Vollmin, J.A.2    Murset, G.3    Curtius, H.4    Prader, A.5
  • 20
    • 0018610873 scopus 로고
    • De Peretti E: 3P-hydroxysteroid dehydrogenase deficiency follow-up study in a girl with pubertal bone age
    • Zachmann M, Forest MG, De Peretti E: 3P-hydroxysteroid dehydrogenase deficiency follow-up study in a girl with pubertal bone age. HormRes 1979:11:292-302.
    • (1979) Hormres , vol.11 , pp. 292-302
    • Zachmann, M.1    Forest, M.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.