NR 507 ADVANCED PATHO EXAM NEW VERSION
UPDATE 2024-2025 BEST STUDYING MATERIAL
WITH VERIFIED ANSWERS.
What is the most common genetic cause of Prader-Willi syndrome? - CORRECT ANSWER A
deletion of a segment of PATERNAL chromosome 15q. The maternal counterpart is methylated via
genomic imprinting.
What is the most common genetic cause of Angelman syndrome? - CORRECT ANSWER A
deletion of a segment of MATERNAL chromosome 15q. The paternal counterpart is methylated via
genomic imprinting.
A child with Prader-Willi syndrome has been hospitalized. Which assessment findings does the
nurse expect with this syndrome? - CORRECT ANSWER Prader-Willi syndrome is characterized
by insatiable hunger that can lead to morbid obesity in childhood. Abnormal, puppetlike gait,
paroxysms of inappropriate laughter, and nonverbal are characteristics seen in Angelman
syndrome.
The nurse is examining an 8-year-old boy with chromosomal abnormalities. Which sign or
symptom suggests the boy has Angelman syndrome? - CORRECT ANSWER Observation shows
jerky ataxic movement
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