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The projects aim is to investigate the intestinal function of patients suffering from Prader-Willi Syndrome. The methods used are ultrasonographic measurement of the rectal diameter and gastrointestinal transit time
Prader-Willi Syndrome (PWS) is a congenital genetical disease characterized by moderate retardation, food-seeking behavior and a serious risk of developing health threatening overweight, low stature, abnormal body composition and a lack of growth- and sex-hormones. They can not live an independent life and are reliant of help from care personnel.
People with PWS react abnormally to signals from their own bodies. E.g. they have a reduced sense of pain and can have a lacking urge to urination despite a full bladder. Most of the patients also have a relatively slow pulse, which can be consistent with a dysfunction in the nervous system (the parasympathetic nervous system) which also has large significance for the bladder- and bowel function.
The Intestinal function in people with PWS is a sparse described subject, which has not been systematically examined in scientific context. We therefore want to examine whether the bowel function in people with PWS are different from the bowel function in healthy people.
The subject is elucidated by a medical examination, a questionnaire, a registration of toilet habits, a measurement of the rectal diameter by an ultrasound scan and a measurement of the colonic transit time.
The results will be compared to findings in normal healthy people. Because no normal material exists for rectal diameter measured by ultrasound, we will establish one.
The result of the project will increase our knowledge of possible bowel dysfunctions such as constipation, in people with PWS and can immediately lead to improved care for and optimized treatment of the patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prader-Willi patients | |||
| Control group | Control group for ultrasound scan |
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| Measure | Description | Time Frame |
|---|---|---|
| Colonic Transit time | Measured ad modum Göteborg | 6 days |
| Rectal diameter | measured by ultrasound scan | 1 day |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with Prader-Willi Syndrome
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| Name | Affiliation | Role |
|---|---|---|
| Louise K Frandsen, Stud.med | Centre of Rare Diseases, Pediatrics department, Aarhus University Hospital Skejby | Principal Investigator |
| Stense Farholt, Ph.D | Centre for Rare Diseases, Pediatrics department, Aarhus University Hospital Skejby | Study Chair |
| Klaus Krogh, DMSc | Medical Hepato-gastroenterological department, Aarhus University Hospital, Aarhus Sygehus | Study Chair |
| Iben M Jønsson, Ph.D | Pediatrics department, Aarhus University Hospital Skejby | Study Chair |
| Jens B Froekjaer, PhD | Department of Radiology, Aalborg Hospital | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre of Rare Diseases, Pediatric department, Aarhus University Hospital Skejby | Aarhus | Aarhus N | 8200 | Denmark |
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| ID | Term |
|---|---|
| D011218 | Prader-Willi Syndrome |
| D003248 | Constipation |
| ID | Term |
|---|---|
| D008607 | Intellectual Disability |
| D019954 | Neurobehavioral Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
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| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D025063 | Chromosome Disorders |
| D030342 | Genetic Diseases, Inborn |
| D000096803 | Imprinting Disorders |
| D009765 | Obesity |
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |