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The Norrie disease is a genetic disease that affects a person's eye and can lead to blindness in male infants at birth or possibly soon after birth. It causes abnormal development of the retina. The retina is the layer of sensory cells that detect color and light, with masses of immature cells that are retinal accumulating at the back of a person's eye. The pupils of the eye later begin to turn white when light is shone on it. This is called leukocaria. The Norrie Disease is a rare disease that can cause deafness as well. Since this genetic disease is rare, it really does not affect a lot of people. Also, this disease usually affects males a lot more than females. Males are affected by loss of vision present at birth or after and females are never really affected by this that often.
- Mariah White, Shaelin Carpenter and Jason Bishop.

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The syndrome is characterized by a mishaped nose, broad thumbs and  the big toes.

90% are affected

Male

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(B0

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(By, Andre Carson and Jonah LaGrand )
-Weak Muscles
-Learning Disabilities
-Big Calves

1 in every 3,500 to 5,000

Primarily affects males but rarely affects females.

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Madison Sloan and Kendra Extine 2) Red/green and blue color blindness is usually passed down from your parents. The gene which is responsible for the condition is carried on the X chromosome. More than 99% of all color blind people are suffering from a red-green color vision deficiency.
3)  1 in 12 men (8%) and 1 in 200 women in the world.
4) More men are affected more than woman.

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1)Hirshsprung's Disease affects the colon of new born babies and toddlers. The disease prevents bowel movement to pass through the intestines do to missing nerve cells.
2) About 1:5000 children born in the United States has Hirschsprung disease.
3) Hirchsprung's disease is more commonly known to affect men more than woman.

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Nonsyndromic Deafness by RJ Gubatan and Austin Hembree

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Nonsyndromic Deafness by RJ Gubatan and Austin Hembree

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(1) What does the nonsyndromic deafness cause or do? Causes hearing loss.
(2)How many individual are affected by the nonsyndromic deafness? Between 2 and 3 per 1,000 children in the United States are born with nonsydromic deafness.
(3) Does nonsyndromic deafness affect one gender more than the other? Both of them are affected the same.

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Spinal and bulbar muscular atrophy: Aqudum, Bethany

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Spinal and bulbar muscular atrophy: Aqudum, Bethany

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2) SBMA is muscle wasting in arms and legs results in arms and legs cramping; leg and muscle weakness also causes difficult walking and constant falling
3) 1 in 150,000
4) occurs more in males rare in females

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It caused by mutation of the enzyme steroid sulfatadse.
It looks like it is wrinkley and looks dried skin.
50% of males
yes, males

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what does it do it makes blood not able to clot,and when they get cut they cant stop the bleeding unless they inject their selves with a protein that their body cant make because of the hemophilia disease.

How many individuals are affected by this. 1 to 5000.

Does it affect one gender more than the other. it can affect both genders but it is rare to affect females.

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Jhadin Smith.
Sydney Elsberry
-It delays activity in brain and a delay in eye sight.
-Then causes of optic horn syndrome is long neck and/or long face, coarse hair, twisting of blood vessel.
- 1/3 family don't have the diprder in their family genes.
- There isn't one certain gender that is affected by the optic horn syndrome.

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What does Hemophilia A cause or do? Hemophilia A is a disorder that doesn't allow the blood to clot normally.

How many individuals are affected by it? 1 in 5,000 male births in the U.S.A

Does it affect one gender more then the other? It Affects men more then females.

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Lowe syndrome can primarily affect the eyes, brain, and kidneys.
Lowe syndrome will mainly be found in guys.
1 and 10 males per 1,000,000 people.

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by: Lindsay & Lucy
Spinal muscular atrophy is a genetic disorder that affects the control of muscle movement. Sma is caused by lost of nerve cells called motor neurons.

1 in 35 people, or nearly 10 million American, unknowingly carries the gene responsible for sma.

Male are more common to get Spinal Muscular Atrophy.