[1] 曾畿生,王德芬.现代儿科内分泌学:基础与临床[M].上海:上海科学技术文献出版社,2001:100,145. [2] Hughes IA,Houk C,Ahmed SF,et al.Consensus statement on management of intersex disorders[J].Arch Dis Child,2006,91(7):554-563. [3] Lee PA,Houk CP,Ahmed SF,et al.Consensus statement on management of intersex disorders[J].Pediatrics,2006,118:488-500. [4] 颜纯,王慕逖.小儿内分泌学[M].北京:人民卫生出版社,2006:755-757. [5] Biason-LauberA.Control of sex development[J].Best Pract Res ClinEndocrinol Metab,2010,24(2):163-186. [6] Bertelloni S,Scaramuzzo RT,Parrini D,et al.Early diagnosis of 5alpha-reductase deficiency in newborns[J].Sex Dev,2007,1(3):147-151. [7] Kossack N,Simoni M,Richter-Unruh A,et al.Mutations in a novel,crypticexon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism[J].PLoS Med,2008,5 (4):e88. [8] Hurme T,Lahdes-Vasama T,Makela E,et al.Clinical findings in prepubertal girls with inguinal hernia with special reference to the diagnosis of androgen insensitivity syndrome[J].Scand J Urol Nephrol,2009,43(1):42-46. [9] Marzuki NS,Suciati LP,Dewi M,et al.Two novel mutations of SRD5A2 gene in indonesian siblings with clinical 5-alpha-reductase deficiency[J].J Pediatr Endocrinol Metab,2010,23(12):1329-1333. [10] Yang Y,Wang BA,Guo QH,et al.Clinical and genetic analysis of three Chinese patients with steroid 5α-reductase type 2 deficiency[J].J PediatrEndocrinol Metab,2012,25(11-12):1077-1082. [11] 邓敏,赵洪福,车与睿,等,真两性畸形1例报告并文献复习[J].中国男科学杂志,2012,26(6):55-56. [12] Barbaro M,Wedell A,Nordenstrom A.Disorders of sex development[J].Semin Fetal Neonatal Med,2011,16(2):119-127. [13] Biason-Lauber A.Control of sex development[J].Best Pract Res ClinEndocrinol Metab,2010,24(2):163-186. [14] Omenice S,Correa RV,Costa EM,et al.Mutations in the SRY.DAXl.SFl and WNT4genes in Brazilian sex-reversed patients[J].Braz J Med Biol Res,2004,37(1):145-150. [15] Knower KC,Kelly S,Ludbrook LM,et al.Failure of SOX9 regulation in 46,XY disorders of sex development with SRY,SOX9 and SF1 mutations[J].PLos One,2011,6(3):e17751. |