Results 81 to 90 of about 8,371 (167)

Male Pseudohermaphroditism with Clitoromegaly in a Dog: Diagnostic Evaluation and Surgical Correction

open access: yes
Background: Hermaphroditism, or intersexuality, is a pathological condition in which an individual possesses both male and female reproductive organs. Hermaphroditism is classified as true or pseudo-hermaphroditism. True hermaphroditism is referred to an
Jovan Spasojevic   +7 more
core   +1 more source

Complex clinico-endocrinological characterization of the idiopathic variant of congenital disorder of sex development in a child with male karyotype 46,XY

open access: yesКлинический разбор в общей медицине
Background. Congenital disorders of sex development (DSD) represent a heterogeneous group of dysontogenetic conditions characterized by a discordance between chromosomal, gonadal, and phenotypic sex.
Svyatoslav M. Yurin   +5 more
doaj   +1 more source

Intra-Abdominal Testicular Seminoma in a Woman with Testicular Feminization Syndrome

open access: yesCase Reports in Radiology, 2011
We report a case of intra-abdominal testicular tumor in a 36-year-old married lady presenting with chief complaints of primary amenorrhea. The patient was later diagnosed with testicular feminization syndrome, a form of male pseudohermaphroditism.
Darshana D. Rasalkar   +4 more
doaj   +1 more source

A case of male pseudohermaphroditism with structural abnormalities of Y chromosome (ring Y) [PDF]

open access: yes, 1988
A case of male pseudohermaphroditism with ring Y chromosome is reported. The patient was a 3-year-old boy with hypospadias and right cryptorchidism. Culture of peripheral lymphocytes demonstrated a chromosomal mosaicism of 45 X/46 X, r (Y). Moreover, the
伏見, 登   +4 more
core  

Persistent Mullerian duct syndrome: A case report and review of the literature

open access: yesAfrican Journal of Paediatric Surgery, 2010
Persistent Mullerian duct syndrome is a rare form of internal male pseudohermaphroditism, in which Mullerian duct derivatives (uterus and fallopian tubes) are present in a genotypic (46XY) and phenotypic male.
Odi Temitope   +2 more
doaj  

Bilateral Sertoli Cell Tumors in a Patient with Androgen Insensitivity Syndrome

open access: yesCase Reports in Obstetrics and Gynecology, 2017
Androgen insensitivity syndrome is the most common cause of male pseudohermaphroditism and the third most common cause of primary amenorrhea. This genetic alteration is a consequence of inherited defects on the X chromosome causing total or partial ...
Roberta Fonseca de Souza   +4 more
doaj   +1 more source

Biopsychosocial variables associated with gender of rearing in children with male pseudohermaphroditism

open access: yes, 2007
Yilmaz, Savas/0000-0003-2540-5808Objective: The effect of parental rearing on gender identity development in children with ambiguous genitalia remains controversial.
Adiyaman, Pelin   +6 more
core   +1 more source

HYSTERECTOMY IN YOUNG MALE

open access: yesPakistan Armed Forces Medical Journal, 2016
Introduction: Disorders of sexual differentiation (DSD) is the term used for neonates without a definite male or female phenotype. Previously, terms like "intersex" and "pseudohermaphroditism” were used for such individuals.
Mohammad Ali   +3 more
doaj   +2 more sources

Male pseudohermaphroditism as a cause of secondary hypertension: a case report

open access: yes, 2010
Seventeen alpha-hydroxylase deficiency (17OHD) syndrome is a rare genetic disorder of steroid biosynthesis causing decreased production of glucocorticoids and sex steroids and increased synthesis of mineralocorticoid precursors.
Rumeyza Kazancioglu   +11 more
core   +1 more source

Dysgeneticus pseudohermaphroditismus masculinus = Dysgenetic Male Pseudohermaphroditism

open access: yes
A szerzők 45,X/46,XY karyotypusú dysgeneticus pseudohermaphroditismus masculinus esetről számolnak be, amelyet fiatal csecsemőkorban diagnosztizáltak. Az újszülött egyhetes korában proximalis hypospadiasis és jobb oldali retentio testis miatt részletes ...
Balogh, Erzsébet   +8 more
core   +1 more source

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