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The purpose of this study is to determine the prevalence of Fabry mutations in patients with left ventricular hypertrophy (moderate to severe), as measured by echocardiography.This study is a screening study
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| left ventricular hypertrophy | Patients with left ventricular hypertrophy will be used. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| blood sampling | Other | Blood sampling will be used. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Determination of the prevalence of Fabry mutations in patients with left ventricular hypertrophy (moderate to severe), as measured by echocardiography | patients with left ventricular hypertrophy will be screened for Fabry mutations, and results will be communicated within four months | At baseline T0 |
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Inclusion Criteria:
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patients with left ventricular hypertrophy
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| Name | Affiliation | Role |
|---|---|---|
| Raymond Vanholder, MD, PhD | University Hospital Ghent, Belgium | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| AZ Imelda | Bonheiden | Belgium | ||||
| AZ Sint-Blasius |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22805550 | Derived | Terryn W, Deschoenmakere G, De Keyser J, Meersseman W, Van Biesen W, Wuyts B, Hemelsoet D, Pascale H, De Backer J, De Paepe A, Poppe B, Vanholder R. Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy. Int J Cardiol. 2013 Sep 10;167(6):2555-60. doi: 10.1016/j.ijcard.2012.06.069. Epub 2012 Jul 16. |
| Label | URL |
|---|---|
| website of University Hospital Ghent, Belgium | View source |
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| ID | Term |
|---|---|
| D017379 | Hypertrophy, Left Ventricular |
| D000795 | Fabry Disease |
| ID | Term |
|---|---|
| D006332 | Cardiomegaly |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D006984 | Hypertrophy |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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| Dendermonde |
| Belgium |
| AZ Sint-Lucas | Ghent | Belgium |
| Maria Middelares | Ghent | Belgium |
| University Hospital Ghent | Ghent | Belgium |
| Jan Yperman Ziekenhuis | Ieper | Belgium |
| AZ Oostkust | Knokke-Heist | Belgium |
| ZOL | Limbourg | Belgium |
| AZ Zusters van Barmhartigheid | Ronse | Belgium |
| D020763 |
| Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D013106 | Sphingolipidoses |
| D020140 | Lysosomal Storage Diseases, Nervous System |
| D020739 | Brain Diseases, Metabolic, Inborn |
| D001928 | Brain Diseases, Metabolic |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D059345 | Cerebral Small Vessel Diseases |
| D002561 | Cerebrovascular Disorders |
| D014652 | Vascular Diseases |
| D040181 | Genetic Diseases, X-Linked |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008661 | Metabolism, Inborn Errors |
| D008064 | Lipidoses |
| D008052 | Lipid Metabolism, Inborn Errors |
| D016464 | Lysosomal Storage Diseases |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D052439 | Lipid Metabolism Disorders |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |