Results 201 to 210 of about 1,908,985 (246)

Familial Complete Androgen Insensitivity Syndrome (Morris Syndrome or Testicular Feminization Syndrome) in 2 Sisters

Advances in Anatomic Pathology, 2008
OVERVIEWDiagnoses: Familial complete androgen insensitivity syndrome (Morris syndrome or testicular feminization syndrome).Case ID and referral sources: Case 1. Bisceglia's contribution: AMR Seminar no. 48, case 3A. Contributor's file no. 95357-5. Case 2.
Gaetano Magro, Michele Bisceglia
exaly   +4 more sources

Morris Syndrome

2008
exaly   +2 more sources

Cancer of the Urinary Bladder Neovagina in a Patient with Morris’ Syndrome

Onkologie, 2008
Vaginal agenesis is a rare condition, therefore the incidence of a malignant transformation in the neovagina is extremely low.We report on a 42-year-old patient with Morris' syndrome and urinary bladder neovagina with a history of prolonged infections of the urinary bladder and intertrigo of the perineal region.
Mirosław Zbigniew Wielgoś, Iwona Szymusik, Banaszek, A., Barbara Ewa Suchońska, Paweł Kamiński, Halina Gadomska, Leszek Bablok   +6 more
openaire   +2 more sources

[The testicular feminization syndrome (Morris' syndrome)].

Akusherstvo i ginekologiia, 1999
The syndrome of testicular feminization is characterized by female phenotype in the presence of male gonads and has a population frequency of 1:20,000 to 1:60,000. The authors report of 2 cases with this syndrome. Its rarity, diagnostic evaluation and follow-up by the gynecologist are of interest.
P, Delev, S, Pancheva
openaire   +1 more source

[Sex change in children with Morris syndrome].

Archivos espanoles de urologia, 1990
Eleven boys with Morris syndrome underwent feminizing genitoplasty utilizing a segment of the sigmoid colon for neovaginal reconstruction. Bilateral orchiectomy was performed for cosmetic reasons and to prevent neoplasms. Patient follow-up ranging from 6 months to 13 years have demonstrated good results were obtained.
Domini R., Paico Vilchez E., Lima M., Luca Ceccarelli P., Zumaeta Luna L., Ruggeri G., Grandi M.   +6 more
openaire   +2 more sources

Videolaparoscopic orchidectomy in Morris Syndrome

1994
tecnica di orchiectomia VL nella sdr.
SAVIANO, Massimo, PICCOLI M, HEYDARI A, GELMINI, Roberta   +3 more
openaire   +1 more source

Laparoscopic Surgery - A Feasible Treatment in Morris Syndrome

Acta Endocrinologica (Bucharest), 2011
Morris Syndrome is a pathological condition which needs a special approach regarding both diagnosis and treatment because of its rarity. While the diagnosis is based on karyotype test, the treatment should follow the idea of harmless and cosmetic benefits as well as complete gonads removal.
openaire   +1 more source

Videolaparoscopic bilateral orchidectomy in Morris Syndrome

1995
VL bilateral orchiectomy in Morris ...
SAVIANO, Massimo, PICCOLI M, HEYDARI A, GELMINI, Roberta   +3 more
openaire   +1 more source

[Four cases of Morris syndrome a familial study].

Revue francaise de gynecologie et d'obstetrique, 2007
A case of feminizing testicle in a family with 9 children, of which girls, has been reported by the authors. A familial study showed 4 out of the 7 girls to be affected by the same disease. The mother, aged 81, presented with no anomaly, save the absence of pubic hair.
M, Vitse, C, Vendrely, J C, Boulanger, F, Devimes   +3 more
openaire   +1 more source

Morris’ Syndrome

Acta Endocrinologica (Bucharest), 2015
openaire   +1 more source