Novel variant in MYH9 in a child with proteinuria and thrombocytopenia: a case report and literature review
There is a lack of awareness of the diagnosis and treatment of MYH9-related disorder (MYH9-RD), which is an autosomal dominant disease with heterogeneous clinical manifestations. We summarized the clinical phenotype and reported a novel variant in MYH9 in a child with focal segmental glomerulosclero...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Frontiers Media S.A.
2025-05-01
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| Colección: | Frontiers in Pediatrics |
| Materias: | |
| Acceso en línea: | https://www.frontiersin.org/articles/10.3389/fped.2025.1502727/full |
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