1.A case of incomplete testicular feminization syndrome.
Yong Suck YOUNG ; Soo Hyung SEO ; Young Woo SHIN ; Tae Seung CHO ; Dong Han BAE ; Seung Ha YANG
Korean Journal of Obstetrics and Gynecology 1993;36(7):2389-2397
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
2.A case of incomplete testicular feminization syndrome.
Yong Suck YOUNG ; Soo Hyung SEO ; Young Woo SHIN ; Tae Seung CHO ; Dong Han BAE ; Seung Ha YANG
Korean Journal of Obstetrics and Gynecology 1993;36(7):2389-2397
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
3.A case of testicular feminization syndrome.
Dong Hoon KIM ; Jin Wan PARK ; Tai Young HWANG ; Hyun Ho KIM ; Won Ki LEE
Korean Journal of Obstetrics and Gynecology 1993;36(7):2377-2382
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
4.A case of testicular feminization syndrome.
Dong Hoon KIM ; Jin Wan PARK ; Tai Young HWANG ; Hyun Ho KIM ; Won Ki LEE
Korean Journal of Obstetrics and Gynecology 1993;36(7):2377-2382
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
5.A case of complete testicular feminization syndrome.
Nack Woo LEE ; Ji Young PARK ; Dong Oh KIM ; Kab Soon JU
Korean Journal of Obstetrics and Gynecology 1993;36(12):3960-3964
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
6.A case of complete testicular feminization syndrome.
Soon Do HONG ; Jae Kyoung SONG ; Mu weon LEE ; Wha Suk LIM ; Jong Hak LEE ; Soon LEE
Korean Journal of Obstetrics and Gynecology 1993;36(5):705-710
No abstract available.
Androgen-Insensitivity Syndrome*
;
Male
7.Beyond the X's and Y's: A case of complete androgen insensitivity syndrome
Lipana Ma. Katherine R. ; Tanangonan Gladys G.
Philippine Journal of Reproductive Endocrinology and Infertility 2009;6():1-9
The Sex or sexuality is very complex subject. From a biological standpoint, the appearance of the external genitalia is only one parameter. Complete androgen insensitivity syndrome (CAIS), the most common form of male pseudohermaphroditism, embodies the multifaceted nature of this concept. Patients usually present with 46, XY karyotype with bilateral testes, female external genitalia, a shortened vagina, absent or rudimentary mullerian derivatives, normal breast development, and absent or scant pubic and axillary hair, as was the case in the patient presented herein. Prevalence ranges from 1 :20,400 to 1 :62,400 births. Its management often requires a multidisciplinary approach. Aside from addressing health risks, the psychosexual, social and ethical aspects of this condition should also be dealt with.
ANDROGEN INSENSITIVITY SYNDROME
8.A Case of Androgen Insensitivity Syndrome with Intraabdominal Testes in a 62 year old woman
Kesiah Keren Bugante-Mercado ; Leedah Ranola - Nisperos
Philippine Journal of Reproductive Endocrinology and Infertility 2018;15(1):9-15
Androgen Insensitivity Syndrome (AIS) is a disorder wherein a patient presents with a female
phenotype but is actually genetically male with an XY karyotype. Typically, AIS is diagnosed
at the beginning of second decade, when a phenotypically female patient complains of
amenorrhea. It is extremely rare to make a first diagnosis of AIS after the fifth decade of life.
This case report presents a 62-year old female who consulted because of primary amenorrhea
and intraabdominal mass. Patient was diagnosed with Complete Androgen Insensitivity
Syndrome based on physical exam findings, imaging studies, endocrine tests and karyotyping.
She underwent exploratory laparotomy, adhesiolysis and bilateral orchiectomy. This report
will discuss diagnosis and appropriate management of patients with Complete Androgen
Insensitivity.
Androgen-Insensitivity Syndrome
9.Complete Androgen Insensitivity in two Filipino siblings: A case report
Vanessa S. Ediza ; Alistair Kashmir C. De la Cruz ; Mae Rhea Lim-Pacoli ; Albert L. Chu
Philippine Journal of Internal Medicine 2021;59(4):327-334
Androgen insensitivity syndrome is an X-linked recessive condition resulting in a failure of normal masculinization of the external genitalia in a chromosomally male individual. We describe two phenotypically female siblings aged 27 and 18 years, who presented with primary amenorrhea. The older sibling first consulted because of her desire to be pregnant while her younger sibling consulted upon the physician’s advice. Clinical presentation, physical examination, hormonal and imaging studies and a male (46XY) karyotype confirmed the diagnosis of Complete Androgen Insensitivity Syndrome (AIS) in both individuals. Both of them underwent exploratory laparotomy with histopathology confirming presence of immature testicular tissue. Hormone replacement therapy was then started. Both were advised to undergo psychosocial counseling and both chose to be women. This case report is significant since there are only a few local case reports about siblings presenting with this condition.
Androgen-Insensitivity Syndrome
;
Karyotyping
10.Familial androgen insensitivity syndrome detected in four siblings in a family.
Hae Sung CHO ; Bo Hoon OH ; Sung Wha HONG
Korean Journal of Obstetrics and Gynecology 1992;35(11):1691-1698
No abstract available.
Androgen-Insensitivity Syndrome*
;
Humans
;
Male
;
Siblings*