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How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease?
Mucopolysaccharidosis type I (MPS I) is a hereditary metabolic disease that manifests itself in childhood by systemic damage to tissues and organs, a constantly progressive course leading to disability. Diagnosis of mild forms of the disease is particularly difficult due to the absence of specific s...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
"Paediatrician" Publishers LLC
2019-01-01
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| Col·lecció: | Voprosy Sovremennoj Pediatrii |
| Matèries: | |
| Accés en línia: | https://vsp.spr-journal.ru/jour/article/view/1979 |
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