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U01.17.008 Prader–Willi syndrome
←
U01.17.007 Marfan syndrome
U01.17.009 Angelman syndrome
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Exam Questions
,
U01.17 Review condition and pathophysiology
,
USMLE Step 1 Review
8 Total attempts
15q11-q13 deletion
,
behavioral problems
,
endocrine features
,
genetic disorder
,
hyperphagia
,
hypogonadism
,
hypotonia
,
imprinting disorders
,
intellectual disability
,
Medical Flashcards
,
neonatal hypotonia
,
obesity
,
paternal deletion
,
Pediatric Genetics
,
Prader-Willi Syndrome
,
Prader–Willi complications
,
Prader–Willi diagnosis
,
Prader–Willi review
,
Prader–Willi study
,
short stature
,
USMLE Step 1
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