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Prader-Willi syndrome - All Information

Definition of Prader-Willi syndrome:

Prader-Willi syndrome is disease that is present from birth (congenital). People with this condition are obese, have reduced muscle tone and mental ability, and have sex glands that produce little or no hormones.

Causes, incidence, and risk factors:

Prader-Willi syndrome is caused by a gene missing on part of chromosome 15. Normally, your parents each pass down a copy of this chromosome. Most patients with Prader-Willi syndrome are missing the genetic material on part of the father's chromosome. The rest of patients with this condition often have two copies of the mother's chromosome 15.

The genetic changes occur randomly. Patients usually do not have a family history of the condition.

Symptoms:

Newborns with this disorder:

  • Are small for gestational age
  • Have genitals that are not well developed (in boys, the testicles cannot be felt in the scrotum)
  • Have problems sucking and swallowing, and often do not gain weight
  • May seem floppy and feel like a "rag doll" when held
  • Often have a weak cry
  • Show changes in the face, such as "almond-shaped" eyes and a small, downturned mouth

Other symptoms include:

  • Irregular areas of skin that look like bands, stripes, or lines
  • Llimb (skeletal) abnormalities
  • Very small hands and feet compared to the body

Affected children have an intense craving for food and will do almost anything to get it. This results in uncontrollable weight gain and morbid obesity. Morbid obesity may lead to lung failure, which includes low blood oxygen levels, right-sided heart failure, and death.

Signs and tests:

Signs of Prader-Willi syndrome may be seen at birth. Newborns with the condition are often small and very floppy. Male infants may have undescended testicles.

As the child grows older, laboratory tests may show signs of morbid obesity, such as:

  • Abnormal glucose tolerance
  • Above normal level of the hormone insulin in the blood
  • Failure to respond to luteinizing hormone releasing factor
  • High carbon dioxide levels
  • Lack of oxygen supply

There may also be signs of right-sided heart failure and knee and hip problems.

Treatment:

Infants may need a feeding tube to help with weight gain.

Obesity is the greatest threat to health. Limiting calories will control the obesity but the family, neighbors, and school must work together closely, because the child will try to get food wherever possible. Exercise can increase lean body mass in children with Prader-Willi syndrome.

Growth hormone has also been shown to improve physical strength and agility in patients with Prader-Willi syndrome. There have been some concerns about the effect of GH on lung function in children with this condition. Parents should discuss the possible side effects with the child's doctor.

A very small penis in the male infant may be corrected with testosterone.

Low levels of sex hormones may be corrected at puberty with hormone replacement.

Children with this condition will need behavioral therapy.

Support Groups:

For additional resources and support, see:

  • Prader-Willi Alliance -- www.prader-willi.org
  • Prader-Willi Syndrome Association -- www.pwsausa.org

Expectations (prognosis):

The person will need the right education for his or her IQ level. Controlling weight will allow for a much more comfortable and healthy life.

Complications:

  • Bone (orthopedic) problems
  • Diabetes
  • Right-sided heart failure

Calling your health care provider:

Call your health care provider if your child has symptoms of this condition. The disorder is frequently suspected at birth.

  • Reviewed last on: 5/1/2011
  • Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

References

Saitta SC, Ackai EH. Specific chromosome disorders in newborns. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 20.

McCandless SE; Committee on Genetics. Clinical report -- health supervision for children with Prader-Willi syndrome. Pediatrics. 2011; 127(1):195-204.

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