Mueller-Weiss syndrome

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Overview

Mueller-Weiss syndrome (also called Brailsford-Müller-Weiss syndrome or spontaneous osteonecrosis of the navicular in adults) is a rare condition affecting a small bone in the foot called the navicular bone. This bone sits in the middle of the foot and plays an important role in walking and bearing weight. In Mueller-Weiss syndrome, the navicular bone slowly loses its blood supply, causing the bone tissue to break down and the bone to collapse or fragment over time. This process is called avascular necrosis or osteonecrosis. The condition mainly affects middle-aged adults, especially women, and usually causes pain on the inner side of the midfoot that gets worse with walking or standing. The foot may become swollen, tender to the touch, and the arch of the foot can flatten or change shape. Symptoms often develop gradually and can be mistaken for other foot problems, which sometimes delays diagnosis. Treatment ranges from conservative options like rest, custom shoe inserts (orthotics), and pain medications to more involved treatments like immobilization in a cast or boot. In more severe cases, surgery may be needed to stabilize or fuse the affected bones. While the condition is not life-threatening, it can significantly affect a person's ability to walk and stay active. Early diagnosis and treatment are important to slow the progression and preserve foot function.

Also known as:

Key symptoms:

Pain on the inner or top part of the midfootSwelling around the middle of the footTenderness when pressing on the navicular bonePain that gets worse with walking, standing, or physical activityFlattening of the foot archStiffness in the midfootLimping or altered walking patternFoot deformity as the condition progressesDifficulty wearing regular shoesReduced ability to walk long distances

Clinical phenotype terms (21)— hover any for plain English
Foot painHP:0025238Positional foot deformityHP:0005656Limitation of movement at anklesHP:0010505Edema of the dorsum of feetHP:0012098Facet joint arthrosisHP:0030871Abnormality of the os naviculare pedisHP:0100339ChondritisHP:0100662Sclerosis of foot boneHP:0100925Fragmented, irregular epiphysesHP:0005063Knee osteoarthritisHP:0005086Equinovarus deformityHP:0008110Talipes calcaneovarusHP:0008124Joint subluxationHP:0032153Tibiofibular diastasisHP:0100535
Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Mueller-Weiss syndrome.

View clinical trials →

No actively recruiting trials found for Mueller-Weiss syndrome at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Mueller-Weiss syndrome community →

No specialists are currently listed for Mueller-Weiss syndrome.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Mueller-Weiss syndrome.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Mueller-Weiss syndrome

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Caregiver Resources

NORD Caregiver Resources

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Mental Health Support

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Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.What stage is my Mueller-Weiss syndrome, and how quickly might it progress?,What are the best non-surgical options for my level of symptoms, and how long should I try them before considering surgery?,What type of surgery would you recommend for me, and what are the risks and expected outcomes?,Will I need custom orthotics, and how do I get fitted for them?,Are there any activities I should avoid to prevent the condition from getting worse?,How often do I need follow-up imaging to monitor the bone?,Are there any clinical trials or newer treatments I should know about?

Common questions about Mueller-Weiss syndrome

What is Mueller-Weiss syndrome?

Mueller-Weiss syndrome (also called Brailsford-Müller-Weiss syndrome or spontaneous osteonecrosis of the navicular in adults) is a rare condition affecting a small bone in the foot called the navicular bone. This bone sits in the middle of the foot and plays an important role in walking and bearing weight. In Mueller-Weiss syndrome, the navicular bone slowly loses its blood supply, causing the bone tissue to break down and the bone to collapse or fragment over time. This process is called avascular necrosis or osteonecrosis. The condition mainly affects middle-aged adults, especially women, a

How is Mueller-Weiss syndrome inherited?

Mueller-Weiss syndrome follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Mueller-Weiss syndrome typically begin?

Typical onset of Mueller-Weiss syndrome is adult. Age of onset can vary across affected individuals.