Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene

Fertility and Sterility

Volumn 74, Issue 1, 2000, Pages 182-183

  Chen, Chih Ping ^a   Chern, Schu Rern ^a   Chen, Be Fong ^a   Wang, Wayseen ^a   Hwu, Yuh Ming ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE PHOSPHATASE PLACENTA ISOENZYME; ANDROGEN RECEPTOR;

ADOLESCENT; ANDROGEN INSENSITIVITY SYNDROME; CLINICAL ARTICLE; CYTOGENETICS; FEMALE; GENE MUTATION; HAMARTOMA; HUMAN; LAPAROSCOPY; LEYDIG CELL; PRIORITY JOURNAL; SERTOLI CELL; SHORT SURVEY;

EID: 0033944253     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0015-0282(00)00554-9     Document Type: Article

References (4)

1. Robboy SJ, Bernhardt PF, Welch WR. Pathology of abnormal sexual development. In: Fox H, Wells M, editors. Haines and Taylor obstetrical and gynaecological pathology, 4th ed. New York: Churchill Livingstone, 1995:1279-97.
2. Gottlieb B., Beitel L.K., Lumbroso R., Pinsky L., Trifiro M. Update of the androgen receptor gene mutations database. Hum Mutat. 14:1999;103-114.
3. Knoke I., Jakubiczka Ottersen T., Göppinger A., Wieacker P. A(870)E mutation of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and Sertoli cell tumor. Cancer Genet Cytogenet. 98:1997;139-141.
4. Rutgers J.L., Scully R.E. The androgen insensitivity syndrome (testicular feminization) a clinicopathological study of 43 cases . Int J Gynecol Pathol. 10:1991;126-144.