Generalities Flashcards
2 hormones that is secreted by the testes
Testosterone
Mullerian-inhibiting factor
What enzyme converts testosterone to dihydrotestosterone?
5-a-reductase
Absence of mullerian-inhibiting factor causes ____
Uterus
Cervix
Oviducts
Upper 1/3 of vagina
Wolfian duct regress in the absence of ____
testosterone
The presence of ___ chromosome is the single most determinant of sex
Y
Mesonephric duct
Wolfian duct
Paramesonephric duct
Mullerian duct
Hypothesis wherein one X chromosome present in females is inactivated
Lyon hypothesis
sex chromatin mass
barr body
Found in nucleus of neutrophils in females
Drumstick appendages
What is detected in hair root test?
Fluorescent body (Y body)
Gold standard for sex determination
Karyotyping
AOG where all embryos have bipotential gonads
4-6 wks AOG
Cells that secrete testosterone
Leydig cells
Cells that secrete antimullerian hormone
Sertoli cells
AOG when testes descends through inguinal ring
7-9 mos AOG
Sertoli cells develop at ___ wks
6-7
Leydig cells develop at ___
8-9 weeks
2 control mechanisms in devt if phenotypic sex
Classic endocrine mechanism
Local paracrine mechanism
What hormone is required in the diff of external genitalia?
DHT
Genital tubercle develops in to ___ tissue
erectile
M: glans penis, corpus cavernosum
F: clitoris, vestibular bulb
Genital swelling in M fuse to form ___
scrotum and prepuce
Genital swelling in F do NOT fuse but develop into…
labia minora
Urogenital sinus in M develops into…
urethra
cowper’s and prostate gland
Urogenital sinus in F develops into…
urethra
lower 2/3 of vagina
Bartholin’s and Skene’s glands
Genotype for Turner syndrome
XO
Short stature, ovarian dysgenesis, shield chest with widely spaced nipples, webbed neck, coarctation of the aorta
Turner syndrome
Testicular atrophy, eunichoid body shape, tall long extremities, gynecomastia, female hair distribution
Klinefelter syndrome
Genotype of Klinefelter syndrome
47, XXY
2 barr bodies, menstrual irregularities and learning d/o’s
Superfemale (XXX)
Type of hermaphroditism with functional gonads
True hermaphroditism
Genetic males with female phenotype
Male pseudohermaphrodites
Causes adrenal androgen overproduction in the fetus
Congenital adrenal hyperplasia/
21 hydroxylase deficiency
Sex determination established by genetic inheritance
Chromosomal/ genetic sex