familial hemophagocytic lymphohistiocytosis 2

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.

Also known as: FHL2, HLH2, HPLH2, PRF1 genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis type 2, genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1

Category: General

What is familial hemophagocytic lymphohistiocytosis 2?

familial hemophagocytic lymphohistiocytosis 2 is a recognized medical condition. This page explains what it is, symptoms that may accompany it, and the lab tests healthcare providers sometimes use to investigate it. It is educational information only and is not a diagnosis.

If you think you may have familial hemophagocytic lymphohistiocytosis 2, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with familial hemophagocytic lymphohistiocytosis 2

EdemaFailure to thriveFeverJaundiceRecurrent feverSeizureSkin rash

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.