Overview
Legg-Calvé-Perthes disease (LCPD), also known as Perthes disease, coxa plana, or avascular necrosis of the femoral head in children, is a childhood hip disorder in which the blood supply to the femoral head (the ball-shaped top of the thighbone) is temporarily disrupted. This loss of blood flow causes the bone to die (osteonecrosis), weaken, and eventually fragment. Over time, the body attempts to resorb the dead bone and replace it with new bone through a process of revascularization and reossification. The disease primarily affects the musculoskeletal system, specifically the hip joint, and predominantly occurs in children between the ages of 4 and 10 years. Boys are affected approximately four to five times more frequently than girls. Key symptoms include hip pain (which may also be referred to the groin, thigh, or knee), limping, reduced range of motion in the affected hip, and leg-length discrepancy. The condition is unilateral in approximately 85-90% of cases. The severity of the disease depends on the extent of femoral head involvement and the age of onset; younger children generally have better outcomes because they have greater potential for femoral head remodeling. If the femoral head does not heal in a spherical shape, it can lead to early-onset osteoarthritis of the hip in adulthood. The exact cause of Legg-Calvé-Perthes disease remains unclear, though it is considered multifactorial, with potential contributions from genetic susceptibility, thrombophilia, and environmental factors. Treatment depends on the child's age, the degree of femoral head involvement, and the stage of the disease. Conservative management includes activity modification, physical therapy, anti-inflammatory medications, and the use of braces or casts to keep the femoral head well-seated within the acetabulum (containment). Surgical options, such as femoral or pelvic osteotomy, may be considered in older children or those with more severe involvement to improve containment and promote spherical remodeling of the femoral head. Long-term follow-up is essential to monitor hip joint development and function.
Also known as:
Clinical phenotype terms— hover any for plain English:
Multifactorial
Caused by a mix of several genes and environmental factors
Childhood
Begins in childhood, roughly ages 1 to 12
FDA & Trial Timeline
4 eventsSecond Affiliated Hospital, School of Medicine, Zhejiang University — NA
Texas Scottish Rite Hospital for Children
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
No FDA-approved treatments are currently listed for Legg-Calvé-Perthes disease.
4 clinical trialsare actively recruiting — trials can provide access to cutting-edge therapies.
View clinical trials →Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Legg-Calvé-Perthes disease.
Community
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Start the conversation →Latest news about Legg-Calvé-Perthes disease
Disease timeline:
New recruiting trial: PROMIS Evaluation Study
A new clinical trial is recruiting patients for Legg-Calvé-Perthes disease
Caregiver Resources
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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.
Common questions about Legg-Calvé-Perthes disease
What is Legg-Calvé-Perthes disease?
Legg-Calvé-Perthes disease (LCPD), also known as Perthes disease, coxa plana, or avascular necrosis of the femoral head in children, is a childhood hip disorder in which the blood supply to the femoral head (the ball-shaped top of the thighbone) is temporarily disrupted. This loss of blood flow causes the bone to die (osteonecrosis), weaken, and eventually fragment. Over time, the body attempts to resorb the dead bone and replace it with new bone through a process of revascularization and reossification. The disease primarily affects the musculoskeletal system, specifically the hip joint, and
How is Legg-Calvé-Perthes disease inherited?
Legg-Calvé-Perthes disease follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.
At what age does Legg-Calvé-Perthes disease typically begin?
Typical onset of Legg-Calvé-Perthes disease is childhood. Age of onset can vary across affected individuals.
Are there clinical trials for Legg-Calvé-Perthes disease?
Yes — 4 recruiting clinical trials are currently listed for Legg-Calvé-Perthes disease on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.
Which specialists treat Legg-Calvé-Perthes disease?
25 specialists and care centers treating Legg-Calvé-Perthes disease are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.