AN INHERITED INFLAMMATORY DISORDER

Familial Mediterranean Fever

An inherited inflammatory disorder causing recurrent episodes of fever, abdominal pain, chest pain and joint inflammation. Effectively managed with specific long-term medical therapy.

Familial Mediterranean fever (FMF) evaluation in Hyderabad
Inherited GENETIC DISORDER
Recurrent Attacks TYPICAL PATTERN
Treatable WITH SPECIFIC THERAPY

ABOUT THIS CONDITION

What is Familial Mediterranean Fever

Familial Mediterranean Fever (FMF) is an inherited inflammatory disorder characterised by recurrent episodes of fever and inflammation, typically affecting the lining of the abdomen, chest and joints. It is most common in people of Mediterranean and Middle Eastern origin (Sephardic Jews, Armenians, Arabs, Turks) but can occur in other populations. It usually begins in childhood or young adulthood. Typical features include episodes lasting 1 to 3 days of high fever, severe abdominal pain mimicking surgical conditions, chest pain due to pleural inflammation, joint pain and swelling (particularly knees and ankles), and skin rash. Between attacks, patients are usually completely well. Untreated FMF can lead to amyloidosis — deposition of abnormal protein in organs, particularly the kidneys, causing chronic kidney disease. Diagnosis is based on clinical features, ethnic background, family history and genetic testing. Specific long-term medical therapy effectively prevents attacks in most patients and significantly reduces the risk of amyloidosis. Dr. Patnam Pravallika Reddy provides initial evaluation and co-management with rheumatology at Lux Hospitals, Hyderabad.

SIGNS TO WATCH

Common Symptoms

⚠️

Symptoms that need attention

Recurrent episodes of high fever lasting 1 to 3 days Severe abdominal pain mimicking surgical emergency Chest pain due to inflammation of the chest lining Joint pain and swelling — particularly knees and ankles Skin rash, particularly on the lower legs Complete wellness between attacks Risk of amyloidosis with kidney damage if untreated

WHY IT HAPPENS

Causes & Risk Factors

CLINICAL DETAILS

KeyFacts

Diagnosis

Clinical features, ethnic background, family history and genetic testing for MEFV mutations

Pattern

Attacks lasting 1 to 3 days with complete wellness between

Treatment

Specific long-term medical therapy effectively prevents attacks

Amyloidosis

Major long-term complication — preventable with regular therapy

Specialist care

Rheumatology co-management essential

Hospital

Available at Lux Hospitals, Hyderabad — co-managed with rheumatology

HOW WE TREAT IT

Treatment Approach

Specific Long-Term Therapy Prevents Attacks & Amyloidosis

The most effective approach is daily specific long-term medical therapy that prevents acute attacks in most patients and significantly reduces the risk of amyloidosis — the most serious long-term complication. Regular monitoring of kidney function is essential.

  1. 1

    Consultation & Assessment

    Dr. Pravallika reviews symptoms, family history and ethnicity, examines the patient and arranges blood tests and genetic testing.

  2. 2

    Treatment Planning

    A personalised plan is created in coordination with rheumatology, including long-term preventive medical therapy.

  3. 3

    Medical Management

    Daily specific medical therapy to prevent attacks, treatment of acute attacks, regular monitoring of kidney function and management of complications.

  4. 4

    Recovery & Follow-up

    Long-term follow-up with rheumatology including monitoring of attacks, kidney function and treatment adherence.

AVAILABLE TREATMENTS

Treatment Options

Daily Specific Preventive Medical Therapy (Referral for rheumatology)

Daily specific medical therapy effectively prevents acute attacks in most patients and significantly reduces the risk of amyloidosis.

Treatment of Acute Attacks

Acute attacks are managed with supportive care, hydration, anti-inflammatory therapy and treatment of any complications.

Biological Therapy in Selected Cases

Biological therapy is used in patients who do not respond to or cannot tolerate first-line therapy.

Regular Monitoring of Kidney Function

Regular urine and blood tests detect early signs of amyloidosis affecting the kidneys, allowing prompt treatment intensification.

Genetic Counselling and Family Screening

Family screening identifies affected family members and informs reproductive decisions in affected families.

COMMON QUESTIONS

Frequently Asked Questions

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