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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Veröffentlicht in:	Clinical Pediatric Endocrinology 2011, Vol.20(4), pp.95-98
Hauptverfasser:	Katsumata, Noriyuki, Ishiguro, Akira, Watanabe, Hiroshi
Format:	Artikel
Sprache:	eng
Schlagworte:	autoimmune thyroiditis Case Report Fabry disease globotriaosylceramide hypothyroidism α-galactosidase A
Online-Zugang:	Volltext
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