Ledderhose disease

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2Active trials18Specialists8Treatment centers

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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Ledderhose disease, also known as plantar fibromatosis or morbus Ledderhose, is a benign fibroproliferative disorder affecting the plantar fascia of the foot. It is characterized by the development of firm, nodular growths (fibromas) within the plantar aponeurosis — the thick band of connective tissue on the sole of the foot. These nodules typically develop gradually and may be single or multiple, unilateral or bilateral. The condition is considered part of the spectrum of superficial fibromatoses, which also includes Dupuytren disease (palmar fibromatosis) and Peyronie disease (penile fibromatosis). Indeed, Ledderhose disease frequently co-occurs with Dupuytren disease, and the two conditions share similar pathological features. Patients commonly present with firm, slow-growing nodules on the sole of the foot, most often in the medial arch area. In early stages, the nodules may be painless, but as they enlarge, they can cause significant discomfort during walking or standing, particularly when pressing against weight-bearing surfaces. In more advanced cases, the fibrotic tissue may contract, leading to toe contractures (curling of the toes), although this is less common than the contractures seen in Dupuytren disease of the hand. The condition predominantly affects middle-aged and older adults and is more common in males. Treatment of Ledderhose disease is primarily conservative in early or mild cases and may include cushioned insoles, orthotic devices, physical therapy, and corticosteroid injections to reduce pain and inflammation. Radiation therapy has been used in early-stage disease to slow nodule progression. For refractory or severe cases causing significant functional impairment, surgical excision — including subtotal or total fasciectomy — may be considered, although recurrence rates after surgery can be high. Collagenase injections and cryotherapy have also been explored as treatment options. There is currently no cure, and management focuses on symptom relief and maintaining mobility.

Also known as:

Clinical phenotype terms— hover any for plain English:

Lack of skin elasticityHP:0100679
Inheritance

Multifactorial

Caused by a mix of several genes and environmental factors

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

FDA & Trial Timeline

2 events
Nov 2023Study to Assess EN3835 in the Treatment of Plantar Fibromatosis (Also Known as Ledderhose Disease)

Endo Pharmaceuticals — PHASE3

TrialACTIVE NOT RECRUITING
Jan 2018Ledderhose Disease: Radiotherapy or Not?

University Medical Center Groningen — PHASE3

TrialACTIVE NOT RECRUITING

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

No FDA-approved treatments are currently listed for Ledderhose disease.

2 clinical trialsare actively recruiting — trials can provide access to cutting-edge therapies.

View clinical trials →

Clinical Trials

2 recruitingView all trials with filters →
Phase 32 trials
Ledderhose Disease: Radiotherapy or Not?
Phase 3
Active
· Sites: Groningen · Age: 1899 yrs
Study to Assess EN3835 in the Treatment of Plantar Fibromatosis (Also Known as Ledderhose Disease)
Phase 3
Active
PI: Louis Ortega (Endo Pharmaceuticals) · Sites: Mesa, Arizona; Scottsdale, Arizona +64 more · Age: 1899 yrs

Specialists

18 foundView all specialists →
NG
Nina Green
Specialist
PI on 2 active trials16 Ledderhose disease publications
AC
Alina Constantin
FARMINGTON, CT
Specialist
1 Ledderhose disease publication
RL
Robert A Lefkowitz
Specialist
1 Ledderhose disease publication
JH
John H Healey
Specialist
1 Ledderhose disease publication
JT
Jamie Tersago
Specialist
1 Ledderhose disease publication
JS
Joshua D Schoenfeld
NEW YORK, NY
Specialist
1 Ledderhose disease publication
AH
Anneke de Haan
Specialist
4 Ledderhose disease publications
PW
Paul M N Werker
Specialist
4 Ledderhose disease publications
JL
Johannes A Langendijk
Specialist
4 Ledderhose disease publications
RS
Roel J H M Steenbakkers
Specialist
4 Ledderhose disease publications
MK
M Willemijn Kolff
Specialist
2 Ledderhose disease publications
PT
Peter-Paul van der Toorn
Specialist
2 Ledderhose disease publications
HG
Henk Groen
Specialist
2 Ledderhose disease publications
HL
Hans Paul van der Laan
Specialist
2 Ledderhose disease publications
LO
Louis Ortega
Specialist
PI on 1 active trial2 Ledderhose disease publications
JN
Johanna G H van Nes
Specialist
4 Ledderhose disease publications
AW
A Helen Westenberg
MADISON, WI
Specialist
2 Ledderhose disease publications
LO
Luis Ortega
Specialist
PI on 1 active trial

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 Ledderhose disease.

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Caregiver Resources

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Support, advocacy, and financial assistance for caregivers of rare disease patients.

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Family & Caregiver Grants

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Social Security Disability

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

Common questions about Ledderhose disease

What is Ledderhose disease?

Ledderhose disease, also known as plantar fibromatosis or morbus Ledderhose, is a benign fibroproliferative disorder affecting the plantar fascia of the foot. It is characterized by the development of firm, nodular growths (fibromas) within the plantar aponeurosis — the thick band of connective tissue on the sole of the foot. These nodules typically develop gradually and may be single or multiple, unilateral or bilateral. The condition is considered part of the spectrum of superficial fibromatoses, which also includes Dupuytren disease (palmar fibromatosis) and Peyronie disease (penile fibroma

How is Ledderhose disease inherited?

Ledderhose disease follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Ledderhose disease typically begin?

Typical onset of Ledderhose disease is adult. Age of onset can vary across affected individuals.

Are there clinical trials for Ledderhose disease?

Yes — 2 recruiting clinical trials are currently listed for Ledderhose disease on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.

Which specialists treat Ledderhose disease?

18 specialists and care centers treating Ledderhose disease are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.