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The present study will establish a collection of biological samples from Marfan patients or with associated diseases to be used for research purposes only, with due respect for confidentiality.
Marfan syndrome is an autosomal dominant disease (incidence 1/5000) characterized by ocular, cardiac and skeletal abnormalities. More recently, a decrease in fat and muscle mass has been demonstrated, associated with a decrease in exercise endurance, causing a significant deterioration in the quality of life. Little is known about the pathophysiology of these symptoms. Patients with Marfan syndrome or related diseases are followed at the children's hospital as part of the Rare Diseases Reference Centre (CRMR) for Marfan syndrome at the Toulouse University Hospital. During regular check-up visits, an extra sample of blood and urine will be collected and stored for research utilisation with the patient's consent. The ultimate objective of this collection is to provide available biological resources to facilitate the development of subsequent studies aimed at better characterizing the multisystemic disorders in Marfan syndrome, to understand the pathophysiology of the disease, and to identify biological factors that predict the severity and progression of the disease. The possibility of having systematically collected biological resources will make it possible to answer certain questions more quickly depending on the progress of research.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with Marfan syndrome or related syndromes | Children aged at least 3 years old or adult with Marfan syndrome or related syndromes |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| collection of samples of blood and urine | Biological | extra samples of blood and urine will be collected and stored for research utilisation |
|
| Measure | Description | Time Frame |
|---|---|---|
| Constitution of a biological collection from patients with Marfan or related syndromes. | extra sample of blood and urine will be collected | Day 0 |
| Constitution of a biological collection from patients with Marfan or related syndromes. Collection of samples at inclusion. | extra sample of blood and urine will be collected | during the intervention/procedure/surgery |
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Inclusion Criteria:
Exclusion Criteria:
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Patients followed at the Rare Diseases Reference Centre (CRMR) for Marfan syndrome at the Toulouse University Hospital.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Thomas Edouard, MD, PhD | Contact | 5 34 55 85 55 | 0033 | edouard.t@chu-toulouse.fr |
| Françoise Auriol, PhD | Contact | 5 67 77 10 95 | 0033 | auriol.f@chu-toulouse.fr |
| Name | Affiliation | Role |
|---|---|---|
| Thomas Edouard, MD | University Hospital, Toulouse | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Purpan University Hospital | Recruiting | Toulouse | 31059 | France |
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| ID | Term |
|---|---|
| D008382 | Marfan Syndrome |
| ID | Term |
|---|---|
| D001848 | Bone Diseases, Developmental |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D006330 | Heart Defects, Congenital |
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| ID | Term |
|---|---|
| D014554 | Urination |
| ID | Term |
|---|---|
| D014553 | Urinary Tract Physiological Phenomena |
| D012101 | Reproductive and Urinary Physiological Phenomena |
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extra sample of blood and urine
| D018376 | Cardiovascular Abnormalities |
| D002318 | Cardiovascular Diseases |
| D006331 | Heart Diseases |
| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D030342 | Genetic Diseases, Inborn |
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |