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* **Diagnosis**: Diagnosing PHA involves a combination of tests. Doctors usually start with a thorough medical history and physical exam. They will also look into blood tests, measuring the sodium, potassium, and aldosterone levels in your blood. In PHA, you typically see low sodium, high potassium, and *normal or high* aldosterone levels. Urine tests help assess how well your kidneys are functioning and how they are handling electrolytes. Genetic testing can confirm the diagnosis of type 1 PHA by identifying the specific mutations. For type 2 PHA, it is more complex, and testing will focus on identifying specific genetic markers. It’s also important for the doctor to perform an ECG to assess heart function because high potassium levels can cause heart abnormalities.
