Chromosomal Disorders

Disorders carried on chromosomes #1-22.

• Autosomal

• Sex-linked

• Chromosomal

Disorders carried on sex chromosomes.

• Autosomal

• Sex-linked

• Chromosomal

Tags

NGSS.HS-LS3-2

Will show patterns/evidence on a karyotype.

• Autosomal

• Sex-linked

• Chromosomal

Chromosomal condition(s) resulting from non-disjuction causing a monosomy.

• Turner

• Down

• Klinefelter's

• Edward's

• Colorblindness

Results form malformed cones in the eye which are responsible for sensing color.

• Achondroplasia

• Color-blindness

• Cystic fibrosis

• Huntington's disease

• Phenylketonuria

Female with impacted growth and sexual development complications including fold on back of neck, lack of menstruation, brown spots on body, and lack of breast development.

• Turner

• Down

• Klinefelter's

• Edward's

• Colorblindness

Occurs in 1/1000 individuals. These individuals have distinct facial features as well as some mental delays.

• Turner

• Down

• Klinefelter's

• Edward's

• Colorblindness

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

Individuals develop as males. Subtle charactistics become apparent at puberty when extra breast tissue develops, musculature in body doesn't develop and testes are also impacted.

• Turner

• Down

• Klinefelter's

• Edward's

• Colorblindness

Clotting disorder in which individuals lack an important factor needed for blood to clot.

• Hemophilia

• Albinism

• Cystic fibrosis

• Colorblindness

• Phenylketonuria

Tags

NGSS.HS-LS3-2

Red blood cells do not form properly, instead they cannot carry oxygen properly and may get lodged in areas causing extreme pain.

• Hemophilia

• Albinism

• Sickle cell disease

• Colorblindness

• Phenylketonuria

Tags

NGSS.HS-LS3-2