Bartter disease type 2

Any Bartter syndrome in which the cause of the disease is a mutation in the KCNJ1 gene.

What is Bartter disease type 2?

Bartter disease type 2 is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have Bartter disease type 2, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with Bartter disease type 2

ConstipationDiarrheaFailure to thriveFeverGeneralized muscle weaknessParesthesiaSeizureVomiting

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.