Gastrointestinal Problems in Overweight and Obese Individuals with Prader-Willi Syndrome (P21-033-19)
نویسندگان
چکیده
منابع مشابه
An obese female with Prader-Willi syndrome and daytime sleepiness.
A obese 13-year-old female with Prader-Willi syndrome (PWS) was referred for evaluation of excessive daytime sleepiness. She was a resident of a group home for persons with PWS allowing for dietary management and a regimented schedule. Her daily wake time was 06:30 and bedtime was 21:00. The patient had a tonsillectomy and adenoidectomy at age 5 years for obstructive sleep apnea and had never b...
متن کاملDental Management of Patients with Prader Willi Syndrome
Prader–Willi syndrome (PWS) is a genetic disorder which occurs with a frequency of about one in 10,000–30,000 live newborns. Both males and females, and all races are equally affected. PWS is a complex disorder with multiple disabilities, and the main defect is found in the hypothalamus. Child with PWS at the age between 2 and 3 years becomes constantly hungry and if the diet is not controlled,...
متن کاملMental health problems in children with prader-willi syndrome.
BACKGROUND Prader-Willi Syndrome (PWS) is a genetically determined neurodevelopmental disorder, which occurs in approximately one in 22000 births. AIMS This study aimed to investigate psychiatric characteristics of children diagnosed with PWS compared with an age-, gender- and IQ-matched control group. The parents of children with PWS were assessed for psychological distress in comparison to ...
متن کاملThe assessment of food-related problems in individuals with Prader-Willi syndrome.
OBJECTIVES The objective of this study was to develop an informant-based questionnaire to assess food-related problems in people with Prader-Willi syndrome and to conduct an examination of psychometric properties. DESIGN Following a content analysis of informant interview responses a 16-item questionnaire, the Food Related Problem Questionnaire (FRPQ), with three subscales (preoccupation with...
متن کاملPrader-Willi Syndrome
Prader-Willi syndrome is a neurogenetic disorder characterized by hypotonia and feeding difficulties in infancy, followed by hyperphagia, hypogonadism, mental retardation, and short stature. It was the first recognized microdeletion syndrome identified with high-resolution chromosome analysis, the first recognized human genomic imprinting disorder, and the first recognized disorder resulting fr...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Current Developments in Nutrition
سال: 2019
ISSN: 2475-2991
DOI: 10.1093/cdn/nzz041.p21-033-19