Acknowledgement
Supported by : 보건복지부
References
-
New Ml. Male pseudohermaphroditism due to
$17\alpha hydroxylase$ deficiency. J Clin Invest 1970; 49: 1930 -41 https://doi.org/10.1172/JCI106412 -
손현식, 오용석, 유순집, 윤건호, 강무일, 홍관수 등.
$17\alpha$ -수산화효소 결핍에 의한 남성가성 반음양증 1예. 대한내분비회지 1992; 7: 153-9 -
박창수, 이미리, 정은환, 김정구.
$17\alpha -hydroxylase$ 결핍증에 의한 남성반음양 1예. 대한내분비회지 1993; 8: 363-9 -
김재훈, 최소영, 김장흡, 김진흥, 나종구, 강창석.
$17\alpha -hydroxylase$ 의 결핍으로 인한 남성가성 반음양 1례. 대한산부회지 1997; 40: 896-901 - Berek JS. Novak's gynecology. 13th edition. Philadelphia: Lippincott Williams & Wilkins; 2002
- Leon S, Marc AF. Clinical gynecologic endocrinology and infertility. 7th ed. Philadelphia: Lipincott Williams & Wilkins; 2005
- Matteson SB, Leonard JP, Chung BC. Assignment of the gene for adrenal P450c17 to human chromosome 10. J Clin Endocrinol Metab 1986; 63: 789-91 https://doi.org/10.1210/jcem-63-3-789
-
Chung BC, Picado-Leonard J, Haniu M, Bienkowski M, Hall PF, Shively JE, et al. Cytochrome P450c17 (steroid
$17\alpha -hydroxylase/17,20-layases$ ): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues. Proc Natl Acad Sci USA. 1987; 84: 407-11 - Tvedegaard E, Firederiksen V, Olgaard K, Stamp J. Two cases of 17 alpha-hydroxylase deficiency-one combined with complete gonadal agenesis. Acta EndocrinoI 1981;98:267-73
-
Yanase T, Simpson ER, Waterman MR.
$17\alpha -hydroxylase/17,20-lyase$ deficiency: from clinical investigation to molecular definition. Endocr Rev 1991; 12: 91-108 https://doi.org/10.1210/edrv-12-1-91 -
Heremans GFP, Moolenaar AJ, Van Gelderen HH. Female phenotype in a male child due to
$17\alpha -hydroxylase$ deficiency. Arch Dis Child 1976; 51: 721 -
Kershnar AK, Borut D, Kogut MD, Biglieri EG, Schambelan M. Studies in a phenotypic female with
$17\alpha -hydroxylase$ deficiency. J Pediatr 1976; 89: 395 -400 https://doi.org/10.1016/S0022-3476(76)80535-5 - Rohmer V, Barbot N, Bertrand P. A case of male pseudonennaphroditism due to 17-hydroxylase deficiency and hormone profiles in the nuclear family. J Clin Endocrinol Metab 1990; 71: 523-9 https://doi.org/10.1210/jcem-71-2-523
- Portuondo JA, Neyro JL, Barral A, Gonzalez-Gorospe F, Benito JA. Management of phenotypic female patients with a XY karyotype. J Reprod Med 1986; 31: 611-5
- Kristiansen SB, Doody KJ. Laparosocpic removal of 46XY gonads located within the inguinal canals. Fertil Steril 1992; 58: 1076-7 https://doi.org/10.1016/S0015-0282(16)55466-1
- Kriplani A, Abbi M, Ammini AC, Kriplani AK, Kucheria K, Takkar D. Laparoscopic gonadectomy in male pseudohennaphrodites. Eur J Obstet Gynecol Reprod Biol 1998; 81: 37-41 https://doi.org/10.1016/S0301-2115(98)00143-2