Chapter 6 Flashcards

1
Q

Gender Identity

A

How someone defines their own gender internally

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2
Q

Gender Expression

A

How someone outwardly communicates their gender identity

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3
Q

Gender Roles

A

Culturally defined behaviors seen as appropriate for males or females or nonbinary

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4
Q

What are some physiological differences of male and female?

A

Men have bigger body, bigger brain, etc. Men have higher mortality rates even via pregnancy. Men have higher diseases, accidental death, etc. Women have a lower pain tolerance and more variety in hormones.
Many differences which makes it important for health/medical research to always include women

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5
Q

What are some behavioral differences of male and female?

A

Males are more physically aggressive
Men are not as emotionally expressive as women (react stronger, but keep it in)
Men report masturbating more and wanting more partners
Women are more sexually fluid than men

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6
Q

How many people intersex?

A

1 in 100

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7
Q

What are the Mulleran and Wolffian ducts?

A

The Müllerian ducts are the precursor to the female reproductive tract, and the Wolffian ducts are the precursor to the male reproductive tract.

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8
Q

What does the male embryo secrete at 8-12 weeks?

A

anti-Müllerian hormone (AMH) causing the Müllerian ducts to begin degenerating

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9
Q

cryptorchidism

A

If a male infant has reached three months of age and his testicles have not descended, surgery may be required in order to fully descend them. This is correlated with slightly higher rates of testicular cancer and lower fertility later in life

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10
Q

cloaca

A

the external genitalia of male and female embryos is the same and consists of an anogenital area with a slit (4 wks)

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11
Q

genital swelling

A

precursor to outer labia and scrotum

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12
Q

genital tubercule

A

precursor to clitoris and penis

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13
Q

Klinefelter syndrome

A

affects about 1 in 1,000 newborn infants. It is believed to occur when an ovum containing two or three X chromosomes is fertilized by a Y sperm and thus produces a person with the genotype XXY or XXXY.

these individuals usually have masculine-looking bodies and identify as men. They tend to have smaller penises and testicles, lower testosterone levels, sparse body hair, and higher rates of gynecomastia

Treatment: Testosteronen

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14
Q

Turner syndrome

A

Affects about 1 in 2,000 - 2,500 newborn infants and is usually diagnosed at about age six or seven. It occurs when a person possesses one X chromosome and no Y chromosome, producing the genotype XO.

these individuals have an appearance typically categorized as female and identify as women. Though the symptoms may vary, the most common signs are short/webbed neck, lowered ears, low neck hairline, shortened height, and swollen hands or feet at birth.

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15
Q

XYY syndrome

A

affects about 1 in 1,500 newborn infants and usually results when a typical X-containing ovum is fertilized by a sperm that has two Y chromosomes. Individuals with this syndrome typically experience genital irregularities and decreased fertility, often accompanied by slight cognitive disabilities and, in many cases, autism.

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16
Q

Triple X syndrome

A

affects about 1 in 2,000 newborn infants and results when a typical X ovum is fertilized by a sperm that has an extra X chromosome, producing an embryo with an XXX genotype. Mild cognitive deficits may develop, and fertility is usually low, but many individuals with XXX go undiagnosed.

17
Q

Congenital adrenal hyperplasia (CAH)

A

It occurs when a child lacks an enzyme in the adrenal glands, and as a consequence, these glands release atypically large amounts of androgens in the latter part of fetal development. This may have no effect on an XY fetus, but in an XX fetus, it usually causes partial masculinization of the genitals, leading to an enlarged clitoris and to a partially fused labia and infertility.

18
Q

Androgen insensitivity syndrome (AIS)

A

Affects about one in 13,000 XY fetuses and occurs when the tissues in the XY fetus do not respond to testosterone. As a result, even though the fetus’ gonads produce testosterone, the Wolffian ducts do not respond to it and consequently do not develop into typical male genitalia. Since the testes still produce anti-Müllerian hormone, the Müllerian ducts do not develop into typical female genitalia. As a result, the child typically has a very shallow vaginal pouch, a clitoris, a non-cyclic hormone status, and testes that never descend but continue producing testosterone to which the body cannot respond.

19
Q

​5-Alpha reductase deficiency

A

Very common inn the Dominican Republic (raised as girls then transition to boys)

Born with female or ambiguous genitalia but develop of some secondary sex characteristics

20
Q

Cognitive development theory

A

suggests that children progress through somewhat predictable stages in terms of how they conceptualize gender and that these stages reflect the maturation of their brain and their resulting ability to formulate abstract thought.