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Fabry Disease Superimposed on Overt Autoimmune Hypothyroidism
Fabry disease (FD) is an X-linked recessive disorder caused by lysosomal α-galactosidase A deficiency. FD is characterized by the systemic accumulation of globotriaosylceramide with involvement of the heart, kidney, brain and gastrointestinal system. Recently, nonautoimmune thyroid dysfunction was r...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Japanese Society for Pediatric Endocrinology
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3687644/ https://ncbi.nlm.nih.gov/pubmed/23926402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.20.95 |
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