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K L A AW KR A P E H T INC O W O M O N O C O K R A P ROOSEVELT PRADERWIllI SYNDROMTEHON MAY AWARENESS WALK ASA T UR DAY, M A Y 1 3, 2 0 23PLEASE JOIN US FOR THIS NATIONAL AND LOCAL FUNDRAISING, AWARENESS
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01
First, obtain a thorough medical history and clinical evaluation of the patient.
02
Next, order genetic testing to confirm the diagnosis of Prader-Willi Syndrome.
03
Follow up with additional testing and screenings to monitor the patient's progress and manage any associated health issues.
04
Develop a comprehensive care plan that focuses on addressing the physical, cognitive, and behavioral symptoms of the syndrome.
05
Work closely with a multidisciplinary team of healthcare professionals, including geneticists, endocrinologists, and behavioral specialists, to provide comprehensive care for the patient.

Who needs prader-willi syndrome - genereviews?

01
Individuals showing signs and symptoms of Prader-Willi Syndrome, such as feeding difficulties, poor muscle tone, delayed development, and hyperphagia, may need to be evaluated for the syndrome.
02
Family members of individuals with a confirmed diagnosis of Prader-Willi Syndrome may also benefit from genetic counseling and testing to assess their risk of having a child with the syndrome.
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Prader-Willi syndrome is a complex genetic disorder characterized by feeding difficulties, poor growth, hypotonia, and hypogonadism.
Healthcare providers and researchers working with patients diagnosed with Prader-Willi syndrome are required to file genereviews.
To fill out genereviews for Prader-Willi syndrome, detailed information about the patient's medical history, genetic testing results, and clinical symptoms must be provided.
The purpose of genereviews for Prader-Willi syndrome is to gather comprehensive genetic and clinical data to aid in diagnosis, treatment, and research.
Information on the patient's genetic testing results, growth patterns, psychiatric symptoms, and any associated health issues must be reported on genereviews for Prader-Willi syndrome.
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