Prader-Willi Syndrome (cont.)
In this Article
- Prader-Willi syndrome facts*
- What is Prader-Willi syndrome?
- What are the signs, symptoms, and physical features of Prader-Willi syndrome?
- How common is, and what causes Prader-Willi syndrome?
- Can Prader-Willi syndrome be inherited?
- Where can I find information about treatment for Prader-Willi syndrome?
- Where can I find additional information about Prader-Willi syndrome?
- What other names do people use for Prader-Willi syndrome?
- What if I still have specific questions about Prader-Willi syndrome?
- Where can I find general information about genetic conditions?
Can Prader-Willi syndrome be inherited?
Most cases of Prader-Willi syndrome are not inherited, particularly those caused by a deletion in the paternal chromosome 15 or by maternal uniparental disomy. These genetic changes occur as random events during the formation of reproductive cells (eggs and sperm) or in early embryonic development. Affected people typically have no history of the disorder in their family.
Rarely, a genetic change responsible for Prader-Willi syndrome can be inherited. For example, it is possible for a genetic defect that abnormally inactivates genes on the paternal chromosome 15 to be passed from one generation to the next.
Where can I find information about treatment for Prader-Willi syndrome?
These resources address treatment or management of Prader-Willi syndrome or some of its symptoms.
- DNA Test
- Gene Review: Prader-Willi Syndrome
- MedTerms: Hypotonia
- MedlinePlus Encyclopedia: Prader-Willi syndrome
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