What is Prader–Willi syndrome? a. A genetic disorder characterized by loss of appetite b. Fat accumulation in the liver of leptin-resistant patients c. A failure to adapt to alternating periods of excess and inadequate energy intake d. A genetic disorder resulting in obesity e. Altered receptor activity for ghrelin
What is Prader–Willi syndrome? a. A genetic disorder characterized by loss of appetite b. Fat accumulation in the liver of leptin-resistant patients c. A failure to adapt to alternating periods of excess and inadequate energy intake d. A genetic disorder resulting in obesity e. Altered receptor activity for ghrelin
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
Related questions
Question
What is Prader–Willi syndrome?
a. |
A genetic disorder characterized by loss of appetite
|
|
b. |
Fat accumulation in the liver of leptin-resistant patients
|
|
c. |
A failure to adapt to alternating periods of excess and inadequate energy intake
|
|
d. |
A genetic disorder resulting in obesity
|
|
e. |
Altered receptor activity for ghrelin
|
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