thyroxine has been researched along with Fabry Disease in 2 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Subclinical hypothyroidism is a common finding in patients with Anderson-Fabry disease, showing an excess prevalence as compared to the normal population." | 1.33 | High prevalence of subclinical hypothyroidism in patients with Anderson-Fabry disease. ( Födinger, M; Gessl, A; Hauser, AC; Lorenz, M; Sunder-Plassmann, G; Voigtländer, T, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Faggiano, A | 1 |
| Severino, R | 1 |
| Ramundo, V | 1 |
| Russo, R | 1 |
| Vuolo, L | 1 |
| Del Prete, M | 1 |
| Marciello, F | 1 |
| Lombardi, G | 1 |
| Cianciaruso, B | 1 |
| Colao, A | 1 |
| Pisani, A | 1 |
| Hauser, AC | 1 |
| Gessl, A | 1 |
| Lorenz, M | 1 |
| Voigtländer, T | 1 |
| Födinger, M | 1 |
| Sunder-Plassmann, G | 1 |
2 other studies available for thyroxine and Fabry Disease
| Article | Year |
|---|---|
Thyroid function in Fabry disease before and after enzyme replacement therapy.
Topics: Adult; Algorithms; alpha-Galactosidase; Biomarkers; Case-Control Studies; Enzyme Replacement Therapy | 2011 |
High prevalence of subclinical hypothyroidism in patients with Anderson-Fabry disease.
Topics: Adult; Fabry Disease; Female; Humans; Hypothyroidism; Kidney Diseases; Lysosomal Storage Diseases; M | 2005 |