A Natural History Study in Children With a Type II Collagen Disorder With Short Stature
A Natural History Study in Children With a Type II Collagen Disorder With Short Stature
Recruiting · NCT05408715 · Registry updated 2023-10-02Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Natural History Study in Children With a Type II Collagen Disorder With Short Stature | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Kniest dysplasia, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Strudwick syndrome, bone disorder, connective tissue disorder, cutaneous mucinosis, endocrine system disorder, hereditary disease, hypochondrogenesis, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 4, musculoskeletal system disorder, spondyloepiphyseal dysplasia congenita | Recruiting | Not stated | 2023-10-02 | NCT05408715 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Innoskel | 1 |
2 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Hopital Necker-Enfants Malades | Paris | France | 2 |
| Hospital Universitario La Paz | Madrid | Spain | 75 |