Medicina clinica
The most recent articles from:
June 2021
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Liddle syndrome is an autosomal dominant hereditary disease caused by a single gene mutation. Typical clinical manifestations are early-onset hypertension and hypokalaemia and can be treated using ENaC blockers (amiloride and aminopterin). ⋯ The patient is an atypical case of Liddle syndrome; genetic analysis is helpful and essential for diagnosis.