Familial hypoaldosteronism
Name: |
Familial hypoaldosteronism
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Description: |
A rare genetic hypoaldosteronism that typically presents in infancy (earl-onset familial hypoaldosternism) as a life-threatening electrolyte imbalance (failure to thrive, recurrent vomiting, and severe dehydration). A history of fever, diarrhoea, lethargy, poor weight gain, poor feeding since birth may also be present. Older subjects (late-onset familial hypoaldosteronism) are less severely affected or asymptomatic.
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ORPHAcode: |
427
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XREF(s): | |
Analyte(s): | |
Created: |
04 Feb 2020 - 15:13
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Changed: |
01 Aug 2021 - 06:46
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