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...
| Main Authors: | , , |
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| Format: | Online |
| Language: | English |
| Published: |
The Japanese Society for Pediatric Endocrinology
2011
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687644/ |