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Patients with type III glycogen storage disease (GSDIII) can develop liver fibrosis, which can be complicated by liver failure or even hepatocellular carcinoma. Since the beginning of the 21st century, non-invasive techniques for assessing fibrosis, such as liver elastography, have been developed. These techniques often make it possible to avoid liver biopsies during patient follow-up and have already been validated in the management of several diseases in adults. These techniques are also beginning to be recommended for monitoring certain chronic liver diseases in children.
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| Measure | Description | Time Frame |
|---|---|---|
| Liver elastography values | Liver fibrosis is classified into four stages, from 0 to 4:
| 1 hour after consultation |
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Inclusion Criteria:
Exclusion Criteria:
- Patients monitored for type III glycogen storage disease but who had never undergone liver elastography during their follow-up.
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Patients under 22 years of age
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Camille WICKER, MD | Contact | 33 3 88 12 77 12 | camille.wicker@chru-strasbourg.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Service de pédiatrie 1 - CHU de Strasbourg - France | Recruiting | Strasbourg | 67091 | France |
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| ID | Term |
|---|---|
| D008103 | Liver Cirrhosis |
| D006010 | Glycogen Storage Disease Type III |
| ID | Term |
|---|---|
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D005355 | Fibrosis |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006008 | Glycogen Storage Disease |
| D002239 | Carbohydrate Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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