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[A case of male pseudohermaphroditism with incomplete testicular feminization syndrome].
Hinyokika Kiyo. 1992 Feb; 38(2):233-6.HK

Abstract

A 19-year-old female visited our hospital because of primary amenorrhea. She was genetically (46XY) male. Her breasts were poorly developed. She had no pubic or axillary hair. The phenotype was female, and the vagina had a short and closed end. Plasma testosterone (T) and 5-alpha dihydrotestosterone (DTH) were low. However, DHT was elevated by ex vivo T load. The testis, which was atropic, epididymis and vas deferens, which were well developed, were found and resected by operation. The amount of androgen receptors of the skin tissue of the external genitalia was normal. These findings suggested that male pseudohermaphroditism with incomplete testicular feminization syndrome may have been caused by androgen resistance syndrome due to the disorder of androgen receptor complex, genetic information or post receptor.

Authors+Show Affiliations

Department of Urology, Osaka City University Medical School.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

jpn

PubMed ID

1561963

Citation

Sakamoto, W, et al. "[A Case of Male Pseudohermaphroditism With Incomplete Testicular Feminization Syndrome]." Hinyokika Kiyo. Acta Urologica Japonica, vol. 38, no. 2, 1992, pp. 233-6.
Sakamoto W, Kishimoto T, Nakatani T, et al. [A case of male pseudohermaphroditism with incomplete testicular feminization syndrome]. Hinyokika Kiyo. 1992;38(2):233-6.
Sakamoto, W., Kishimoto, T., Nakatani, T., Gotou, A., Kawano, M., Ameno, Y., & Maekawa, M. (1992). [A case of male pseudohermaphroditism with incomplete testicular feminization syndrome]. Hinyokika Kiyo. Acta Urologica Japonica, 38(2), 233-6.
Sakamoto W, et al. [A Case of Male Pseudohermaphroditism With Incomplete Testicular Feminization Syndrome]. Hinyokika Kiyo. 1992;38(2):233-6. PubMed PMID: 1561963.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [A case of male pseudohermaphroditism with incomplete testicular feminization syndrome]. AU - Sakamoto,W, AU - Kishimoto,T, AU - Nakatani,T, AU - Gotou,A, AU - Kawano,M, AU - Ameno,Y, AU - Maekawa,M, PY - 1992/2/1/pubmed PY - 1992/2/1/medline PY - 1992/2/1/entrez SP - 233 EP - 6 JF - Hinyokika kiyo. Acta urologica Japonica JO - Hinyokika Kiyo VL - 38 IS - 2 N2 - A 19-year-old female visited our hospital because of primary amenorrhea. She was genetically (46XY) male. Her breasts were poorly developed. She had no pubic or axillary hair. The phenotype was female, and the vagina had a short and closed end. Plasma testosterone (T) and 5-alpha dihydrotestosterone (DTH) were low. However, DHT was elevated by ex vivo T load. The testis, which was atropic, epididymis and vas deferens, which were well developed, were found and resected by operation. The amount of androgen receptors of the skin tissue of the external genitalia was normal. These findings suggested that male pseudohermaphroditism with incomplete testicular feminization syndrome may have been caused by androgen resistance syndrome due to the disorder of androgen receptor complex, genetic information or post receptor. SN - 0018-1994 UR - https://www.unboundmedicine.com/medline/citation/1561963/[A_case_of_male_pseudohermaphroditism_with_incomplete_testicular_feminization_syndrome]_ L2 - https://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/117465 DB - PRIME DP - Unbound Medicine ER -