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Prader-Willi Syndrome

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Presentation on theme: "Prader-Willi Syndrome"— Presentation transcript:

1 Prader-Willi Syndrome
Kalena Spinola

2 Description A cogential (present from birth) disease, affecting many parts of the body. People with this condition are often obese, have reduced muscle tone, mental ability, and produce little or no sex hormones.

3 Symptoms Physical Almond Shaped Eyes Short Stature Small Hands & Feet
Behavior Problems Obsessive/Compulsive Actions Depression Quick Temper

4 Symptoms Infants-Childhood Weak Muscle Tone Trouble Eating
Sleep Abnormalities Body Temperature Delayed Motor Development Mental Retardation

5 Symptoms Adolescence-Adulthood Delayed Puberty Obesity Food Cravings
Leads to: Diabetes High Blood Pressure Joint/Lung Problems

6 Effecting Traits Population Affects 1 in 10,000-25,000 births
Occurs in all Races Effects Male & Female Affects 1 in 10,000-25,000 births Life Expectancy Normal

7 Inheritance Chromosome 15 Deletion Alterations Locus: 15q11-q13
Chromosome Partial Deletion Deletion of Entire Chromosome Maternal Disomy Imprinting Defect Chromosome

8 Reproduction Spontaneous genetic disorder Random occurance
Reproduction is normal

9 Causes Normal Development Depends on Chromosome 15
Effects Hypothalamus Region registers feelings of hunger Lack of muscle mass Fewer calories burned-Obesity

10 Treatments/Cures No Whole Cure Various Therapies
Physical, Speech, Occupational, etc Special Feeding TEchniques Strict Diet/Weight Control

11 Additional Information
Most common genetic cause of obesity Can be detected before birth PWS-like disorder can be developed

12 Resources


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