Carregant...
Myhre Syndrome Associated With Dunbar Syndrome and Urinary Tract Abnormalities: A Case Report
Myhre syndrome is a rare condition caused by a mutation in the SMAD4 gene, which leads to a defective TGF-β/BMP signaling, resulting in the proliferation of abnormal fibrous tissues. Clinically, patients with Myhre syndrome manifest with defects of connective tissue (skin, muscles, joints), and card...
Guardat en:
| Publicat a: | Front Pediatr |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7057230/ https://ncbi.nlm.nih.gov/pubmed/32175297 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2020.00072 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|