Results 91 to 100 of about 9,214 (219)

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

Female pseudohermaphroditism.

open access: yesJournal - Newark Beth Israel Hospital, 1998
Patients with female pseudohermaphroditism have female internal genitalia and karyotype (XX) and various degree of external genitalia virilization. External genitalia is musculinized congenitally when female fetus is exposed to excess androgenic environment.
E, CASSORLA   +3 more
  +6 more sources

Consensus statement on the diagnosis, management, and treatment of angioedema mediated by Bradykinin. Part. II: treatment, follow-up, and special situations [PDF]

open access: yes, 2011
Background: There are no previous Spanish guidelines or consensus statements on bradykinin-induced angioedema. Aim: To draft a consensus statement on the management and treatment of angioedema mediated by bradykinin in light of currently available ...
Baeza, M. L.   +17 more
core   +1 more source

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  

Androgen-independent events in penile development in humans and animals. [PDF]

open access: yes, 2020
The common view on penile development is that it is androgen-dependent, based first and foremost on the fact that the genital tubercle forms a penis in males and a clitoris in females.
Baskin, Laurence   +6 more
core   +1 more source

Sex-linked markers facilitate genetic parentage analyses in knobbed whelk broods. [PDF]

open access: yes, 2005
To explore the potential of sex-linked polymorphisms for genetic parentage analyses in natural populations, we have employed a recently discovered "X-linked" microsatellite marker (in conjunction with polymorphic autosomal loci) to deduce biological ...
Avise, JC, Power, AJ, Walker, D
core  

Search of prostatic tissue in 46,XX congenital adrenal hyperplasia [PDF]

open access: yes
OBJETIVOS: Verificar a ocorrência de tecido prostático em pacientes portadoras da forma clássica de hiperplasia congênita das suprarrenais, com cariótipo 46,XX e analisar a sensibilidade e a especificidade do antígeno prostático específico (PSA) das ...
BARONI, Ronaldo   +9 more
core   +1 more source

Psychosocial considerations in the management of late-diagnosed male pseudohermaphroditism

open access: yesThe Turkish Journal of Pediatrics, 1994
Male pseudohermaphroditism (MPH), which causes ambiguous genitalia, rarely presents during adolescence. Herein we report two siblings diagnosed with MPH at the ages of 16 and 12 years and raised unambiguously as girls. Individuals with MPH provide
T Alkin, A Büyükgebiz, A Baykara
doaj  

Isolation and radioimmunoassay of thyroxine-binding globulin (TGB) [PDF]

open access: yes, 1974
Erhardt, F.   +3 more
core   +1 more source

Male Pseudohermaphroditism [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1966
openaire   +2 more sources

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