Prader-Willi syndrome is due to agenetic disorderof chromosome 15.
Many complications of Prader-Willi syndrome are due to obesity.
Although rare, Prader-Willi syndrome is the most common genetic cause of obesity.
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Infants with Prader-Willi syndrome are often behind other children in development.
Between ages 1-6 years the child with Prader-Willi syndrome suddenly develops a tremendous interest in food and starts overeating.
Children gain weight rapidly at this age.
Distinctive Facial Features
Distinctive facial features also identify a child with Prader-Willi syndrome.
The child’s eyes may cross (strabismus).
Treatment of Prader-Willi Syndrome
There is no cure for Prader-Willi syndrome.
However, the physical problems triggered by the syndrome can be managed.
Administering human growth hormone (Genotropin, Humatrope, Norditropin) improves muscle mass and growth.
Also, sex hormone therapy can be given.
National Library of Medicine.
2018 Oct 4;11:579-593. doi:10.2147/DMSO.S141352
National Health Service.Prader-Willi syndrome symptoms.
National Organization of Rare Disorders.Prader-Willi syndrome.
Wooster Community Hospital.7 signs your child may benefit from speech therapy.
Prader-Willi Syndrome Association.What is Prader-Willi syndrome (PWS)?
