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Questions and Answers
Which feature is universally present in Prader-Willi Syndrome?
Which feature is universally present in Prader-Willi Syndrome?
- Hypogonadism (genital hypoplasia; incomplete puberty) (correct)
- Scoliosis/kyphosis
- Delayed motor development
- Increased risk for type II diabetes
What is the prevalence rate of Prader-Willi Syndrome?
What is the prevalence rate of Prader-Willi Syndrome?
- 1 in 5,000 - 1 in 10,000
- 1 in 100,000 - 1 in 150,000
- 1 in 10,000 - 1 in 25,000 (correct)
- 1 in 50,000 - 1 in 75,000
What is the impact of central hypotonia of Prader-Willi Syndrome during infancy?
What is the impact of central hypotonia of Prader-Willi Syndrome during infancy?
- Average IQ - 60
- Lethargy; poor arousal (correct)
- Short, narrow hands with tapering fingers
- Decreased muscle size
What is the average IQ of individuals with Prader-Willi Syndrome?
What is the average IQ of individuals with Prader-Willi Syndrome?
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What is the major cause of morbidity and mortality in Prader-Willi Syndrome?
What is the major cause of morbidity and mortality in Prader-Willi Syndrome?
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When does hyperphagia typically onset in individuals with Prader-Willi Syndrome?
When does hyperphagia typically onset in individuals with Prader-Willi Syndrome?
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What are the medical consequences of hyperphagia in Prader-Willi Syndrome?
What are the medical consequences of hyperphagia in Prader-Willi Syndrome?
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What is the main problem sensing associated with hyperphagia in Prader-Willi Syndrome?
What is the main problem sensing associated with hyperphagia in Prader-Willi Syndrome?
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What is the recommended treatment for hyperphagia in Prader-Willi Syndrome?
What is the recommended treatment for hyperphagia in Prader-Willi Syndrome?
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What is the growth pattern in individuals with Prader-Willi Syndrome at birth?
What is the growth pattern in individuals with Prader-Willi Syndrome at birth?
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