Familial hyperthyroidism due to mutations in TSH receptor
Name: |
Familial hyperthyroidism due to mutations in TSH receptor
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Description: |
A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history.
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ORPHAcode: |
424
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Synonyms: |
Familial non-immune hyperthyroidism
Resistance to thyroid stimulating hormone
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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