Difficulties in the diagnosis of Fabry disease in real clinical practice
Background. Fabry disease is a genetically determined disease in which deficiency or complete absence of α-galactosidase A (GLA/AGAL) activity is formed. Diagnosis of this pathology is difficult, especially in late onset, with predominant cardiac involvement.The aim. Evaluation of specially designed...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Russo |
| Publicado em: |
Scientific Сentre for Family Health and Human Reproduction Problems
2025-03-01
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| coleção: | Acta Biomedica Scientifica |
| Assuntos: | |
| Acesso em linha: | https://www.actabiomedica.ru/jour/article/view/5209 |
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