HUMAN GENETICS Disorders. AUTOSOMAL RECESSIVE zAutosomes =, chromosomes #1- #22

HUMAN GENETICS

Disorders

AUTOSOMAL RECESSIVE

Autosomes = , chromosomes #1- #22

Cystic Fibrosis-ff

It causes the body to produce a thick, sticky mucus that clogs the lungs and digestive tract.

Cystic Fibrosis (cont.)

Most common fatal genetic disease in US today

Most common in Caucasians

Cystic Fibrosis Movie

Cystic Fibrosis

Chromosome 7FF = no CFFf = carrierff = has CF(recessive)

PKU on chromosome 12

Lacks enzyme to break down the amino acid phenylalanine (found in milk)

Phenylketonuria (PKU)

PKU (cont.)

The breakdown products can be harmful to developing nervous systems

Leads to mental retardation. Kate with PKU Movie

PKU

PKUChromosome 12

Put on low protein diet

Avoid phenylalanine

TAY SACHS

Results in degeneration of the nervous system.

Chromosome 15

Highest rate in Eastern European Jews

Tay Sachs (cont)

Lack enzyme to break down fat, accumulates in brain

tt Chromosome 15 NOVA Online | Cracki

ng the Code of Life | Watch the Program Here #3

Tay-Sachs SymptomsSymptoms first appear at 4 to 6 months of age when an apparently healthy baby gradually stops smiling, crawling or turning over, loses its ability to grasp or reach out, and eventuallybecomes blind, paralyzed and unaware of its surroundings. Death occurs by age 4.

Albinism

Inability to manufacture pigments (melanin) in skin and eyes

Autosomal recessive trait

Chromosome 11 (will be in movie)

AUTOSOMAL DOMINANT

Sickle Cell Anemia

Autosomal dominant disease -#11

Red blood cells collapse and clot blood vessels

Found in African-Americans

Sickle-Cells

Normal Red Blood Cells-like a donut

Sickle-cells collapse, hard, clog vessels

Sickle-Cell Anemia

CodominantSS = diseaseAS = carrier (somewhat resistant to

malaria)AA =normal hemoglobinSickle Cell Disease - What Causes Sickle

Cell Disease Video - About.com

Sickle-Cell Complications1.pain episodes 2.strokes 3.increased infections 4.leg ulcers 5.bone damage 6.yellow eyes or jaundice 7.early gallstones 8.lung blockage 9.kidney damage and loss of body water in urine 10.painful erections in men (priapism) 11.blood blockage in the spleen or liver (sequestration) 12.eye damage 13.low red blood cell counts (anemia) 14.delayed growth

Huntington’s Disease

Woody Guthrie’s disease (folksinger 1960’s)

Autosomal dominantDoes not manifest

itself until age 20’s - 30’s

H=dominant disease#4

Huntington’sChromosome 4Atrophy of brainUncontrollable

muscle spasms Huntington's Disease Information - HO

PES - HOPES Video Player (SWF) (segment 4) New Treatment for Huntington's Disea

se - Health Videos - redOrbit

Achondroplasia

Autosomal Dominantchromosome 4

Achondroplasia

Dwarfism

short statureDwarfismshortening of limbs, trident handsprominent forehead,

Average adult male height of 52 inches; average adult female height of 49 inches

FAQ

Can short-statured couples become the parents of average-size children?

AA=deadAa=Achondroplasiaaa=normal

A a

A

a

FAQ

Can short-statured couples become the parents of average-size children?

AA=deadAa=Achondroplasiaaa=normal

AA Aa

Aa aa

A a

A

a

Alzheimer syndrome

Widespread nerve cell dysfunction and cell death, neurotransmitter deficiencies

Dementia HowStuffWorks

Videos "Treating Huntington's Disease"

Alzheimer Syndrome

Autosomal DominantFound on Chromosome 1, or

10, or 14, or 19, or 21APO4, is a cholesterol-carrying protein

linked to development a protein that forms plaque in the brain

Brain Loss

Early or mild stage:

memory loss, especially of recent events difficulty in recalling names and conversations misplacing objects  becoming lost in familiar neighborhoods repeating stories and conversations difficulty in learning new information personality changes decreased motivation and drive easily upset or anxious 

Marfan Syndrome

a connective tissue

disorder, Affects skeleton,

lungs, eyes, heart and blood vessels.

unusually long limbs

affected Abraham Lincoln.

Marfan Syndrome

autosomal dominant disorder

chromosome 15(will be in movie)

SEX-LINKED DISORDERS

On X chromosome

Hemophilia

Hemophilia

Blood does not clot normally

Sex-linked recessive

Missing AHF (clotting factor in blood)

Czar Nicholas royal family

Royal Pedigree-Hemophilia

“bleeder’s disease”

XHXh = female carrier

XhXh = female hemo

XHY = normal male

XhY = hemo male

Color Blindness

More common in males

Sex-linked (red and green on X chromosome)

Blue is on an autosome

Ishihara Test for Color Blindness

Ishihara Test for Color Blindness

The individual with normal color vision will see a 5 revealed in the dot pattern. An individual with Red/Green (the most common) color blindness will see a 2 revealed in the dots.

Color blindness=can’t tell certain colors

Recessive on X chromosome = c

XCXc = normal female (carrier)

XcY = color-blind

male

What numbers do you see?

Note: X and Y used

Need X and Y on Punnetts

Duchenne Muscular Dystrophy

MD

Duchenne Muscular DystrophyOn Xm chromosomeWeakens and degenerates

musclesFound mostly in males

DMD

Onset ·Early childhood - about 2 to 6 years.

Symptoms · Generalized weakness of muscle

Wasting affecting limb and trunk

Leg muscles first. Calves often enlarged.

DMD

Survival rare beyond late twenties.

X-linked recessive (females are carriers).

POLYGENIC DISORDERS

Determination of disorder occurs on more than one chromosome

SPINA BIFIDA

is a fault in the spinal column in which one or more vertebrae (the bones which form the backbone) fail to form properly, leaving a gap or split.

Spina Bifida

#6, #14 and othersGap in spinal

column

Shunts often put in the brain to drain the fluid

Agent Orange

Children with Spina Bifida whose parent was in contact with Agent Orange during the Vietnam War are compensated

Cleft Lip/Cleft Palate

A cleft is an opening in the lip, the roof of the mouth (hard palate) or the soft tissue in the back of the mouth (soft palate).

#11, #17, #22

Clefts

Clefts occur more often among Asians and certain groups of American Indians than among whites. They occur less frequently among blacks.

Cleft lip/palate

As you can imagine there are feeding problems

#11, #22, #17 –polygenic

On Y chromosome

Testes determining factor

Nondisjunction

Chromosomes to segregate unevenly during meiosis

Mistakes in Meiosis

Down’s Syndrome

Trisomy 21Extra fold over

eyeSluggish

musclesMental

problems

Trisomy 21 Karyotype

Nondisjunction

Turner’s Syndrome

Adults with Turner syndrome are short, averaging around four feet, eight inches in height.

But girls with Turner syndrome don't start life as very short individuals - they become short over time-do not develop sexually

Turner’s Syndrome 45 X0

Kleinfelter’s 47 XXY

Kleinfelter’s

Testes are small and fail to produce normal levels of testosterone which leads to breast growth (gynaecomastia) in about 40% of cases and to poorlydeveloped secondary sexual characteristics.

Klinefelter’s

Men are sterile (no sperm).

NOTE:

If you are born with no “X” chromosome- it is fatal

If missing an autosome-it is fatal

Special Topics In Human Genetics

BARR BODIES

When a female is born one of her X chromosomes is inactivated = a Barr Body (early in embryonic development)

Used to test femaledness at Olympics

So there is not excess of X info in females

Calico Cat

Only females have 3 colors (orange, black, white)

Looks like “Pepper”

GENETIC DISORDERS REFERENCE SHEET:Down Syndrome (Trisomy 21)Edward's Syndrome (Trisomy 18)Patau Syndrome (Trisomy 13)Klinefelter Syndrome (47, XXY)

Turner Syndrome (45 XO)

Metafemale (46XXX)-taller

Autosomes (#1-22) so 44 if normal

Angelman Syndrome

Deletion of Chromosome 15If inherited from FATHER Symptoms: Short and obese, delayed

development, frequent laughing

Angelman Syndrome

Prader-Willi Syndrome

Deletion is inherited from mother’s chromosome 15

Hyperactive, chronic hunger, low muscle tone, obesity

Prader-Willi Syndrome

–Before and after controlled eating