Bilateral Sertoli Cell Tumors in a Patient with Androgen Insensitivity Syndrome
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
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]
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
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]
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]
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]
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
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]
Erhardt, F. +3 more
core +1 more source
Male Pseudohermaphroditism [PDF]
openaire +2 more sources

