Biology · Genetic Disorders
Prader-Willi syndrome (PWS), a genetic disorder caused by a loss of function of specific genes on chromosome 15, is clinically characterized by which of the following combinations of symptoms?
- 1Extreme low appetite, microcephaly, hypervigilance, and type 1 diabetes
- 2Insomnia, severe hypertension, immune deficiency, and early baldness
- 3Hyperthyroidism, rapid weight loss, high stature, and excellent cognitive function
- 4Insatiable appetite, obesity, growth hormone deficiency, and intellectual disability✓
Correct answer
Insatiable appetite, obesity, growth hormone deficiency, and intellectual disability
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