Intersex Flashcards
a.The Anatomy of Male and Female Intersex
b.Biological characteristics, commonalities and differences of Male and female
Gender Of Sexuality
A term is used when someone is born with sex characteristics that don’t fit the usual definition of girl or boy.
Intersex
Previously called as having a disorder of sex development (DSD)
Hermaphrodite
How common is being intersex?
✓An estimated 1 in 100 Americans is intersex.
Around 2% of people worldwide have intersex traits.
is a genetic disease that causes biological males to be born with an extra copy of the X chromosome in their cells.
• delay speech and language development in male children
XXY, or Klinefelter syndrome
Males with this condition may not have any symptoms or may have a variety of symptoms, including smaller-than-normal testicles that produce less • May result in infertility
• XXY, or Klinefelter syndrome
XXY Symptoms in young males and teens
• mild dyslexia
• issues with paying attention • lowered energy levels
• difficulty socializing
• delayed puberty, which can include:
• a lack of facial or body hair
• a higher-pitched voice
• more fat deposits around the hips and buttocks, creating a rounder lower half of the body
• enlarged breasts (gynecomastia)
• taller stature than the rest of the family (including long arms and legs) • difficulty increasing or producing muscle tone
• smaller testicles
• smaller penis
XXY Symptoms in adults
•major problems with learning and speech
•poor coordination •unique facial features •bone problems
a genetic condition that occurs when a male has an extra copy of the Y chromosome in each of their cells (XYY). Sometimes, this mutation is only present in some cells. Males with XYY syndrome have 47 chromosomes because of the extra Y chromosome.
• XYY syndrome or Jacob’s syndrome
result of a random mix-up, or mutation, during the creation of a male’s genetic code. syndrome
are not inherited
XYY/ Jacob’s syndrome
result of a random mix-up, or mutation, during the creation of a male’s genetic code. syndrome
are not inherited
XYY/ Jacob’s syndrome
Symptoms of XYY Syndrome
• hypotonia (weak muscle tone)
• delayed motor skill development, such as with walking or crawling
• delayed or difficult speech
• an autism diagnosis
• attention difficulties
• delayed motor skill development, such as with writing • delayed or difficult speech
• emotional or behavioral issues
• hand trembling or involuntary muscle movements • hypotonia (weak muscle tone)
• learning disabilities
• taller-than-average height
Presentation title
XYY symptoms
YOUNG CHILD OR TEENAGER
when chromosomes differ by cell (e.g., some cells are XXY and some are XY)
occurs when a person has two or more genetically different sets of cells in his or her body.
Mosaicism
an organism or tissue where the cells have distinct genomes and all of the cells originated from the same fertilized zygote
Mosaicism
disorders are caused by mosaicism
• Ichthyosis with confetti.
• Klinefelter syndrome.
• Klippel-Trenaunay syndrome.
• Mosaic Down syndrome.
• Pallister-Killian mosaic syndrome.
• Ring chromosome 14 syndrome.
• SOX2 anophthalmia syndrome.
• Triple X syndrome.
• Trisomy 18.
• Turner syndrome.
This is a disorder that causes red, scaly skin all over
Ichthyosis with confetti
. This syndrome can cause low amounts of testosterone. This can lead to problems with sexual development and other issues.
Klinefelter syndrome
• Klippel-Trenaunay syndrome. This disorder causes a red birthmark called a port-wine stain. It also causes excess growth of soft tissues and bones, as well as abnormal veins.
Klippel-Trenaunay Syndrome
is a condition that causes intellectual disabilities and delays, weak muscles, and flat facial features. It can also cause a heart defect, digestive problems, thyroid problems, and other health issues.
Mosaic Down Syndrome
This is a developmental disorder that causes weak muscles, intellectual disability, thin hair, patches of abnormal skin color, and other birth defects.
the body.
Pallister-Killian mosaic syndrome
This condition causes seizures, intellectual disability, and delayed speech and motor development.
Ring Chromosome 14 syndrome
This is a rare disorder that can cause a child to be born without eyes. It can also cause seizures, brain problems, and delayed growth.
SOX2 Anophthalmia Syndrome
This condition is caused by an extra X chromosome in each of a woman’s cells. It can cause learning disabilities, delayed language skills, and problems with motor skills and muscles.
Triple X syndrome
