Multiple epiphyseal dysplasia

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD's medical weight loss NYC, sleep center NYC
Philadelphia medical weight loss and Philadelphia sleep clinics
| Multiple epiphyseal dysplasia | |
|---|---|
| Synonyms | Fairbank's disease |
| Pronounce | |
| Specialty | Medical genetics, Orthopedics |
| Symptoms | Joint pain, early-onset osteoarthritis, short stature |
| Complications | Osteoarthritis, joint deformities |
| Onset | Childhood |
| Duration | Lifelong |
| Types | Ribbing type, Fairbank type |
| Causes | Genetic mutations |
| Risks | Family history |
| Diagnosis | X-ray, Genetic testing |
| Differential diagnosis | Achondroplasia, Spondyloepiphyseal dysplasia |
| Prevention | None |
| Treatment | Physical therapy, Pain management, Surgery |
| Medication | Analgesics, Nonsteroidal anti-inflammatory drugs |
| Prognosis | Variable, depends on severity |
| Frequency | Rare |
| Deaths | |
Multiple Epiphyseal Dysplasia (MED) is a genetic disorder that primarily affects the bones. It is characterized by abnormalities in the growing ends of the bones, known as epiphyses. These abnormalities can lead to a variety of symptoms, including pain, limited mobility, and early-onset osteoarthritis.
Symptoms and Signs[edit]
The symptoms of MED can vary greatly from person to person. Some individuals may have mild symptoms that are barely noticeable, while others may have severe symptoms that significantly impact their quality of life. Common symptoms include:
- Pain in the hips, knees, ankles, and elbows
- Limited range of motion in the affected joints
- Early-onset osteoarthritis
- Short stature
- Abnormalities in the hands and feet, such as clubfoot or flat feet
Causes[edit]
MED is caused by mutations in one of several genes, including COL9A1, COL9A2, COL9A3, COMP, and MATN3. These genes are involved in the formation of cartilage, a flexible tissue that is essential for normal bone growth and development. Mutations in these genes disrupt the normal development of cartilage, leading to the symptoms of MED.
Diagnosis[edit]
The diagnosis of MED is typically based on a combination of physical examination, medical history, and imaging studies. X-rays can reveal characteristic abnormalities in the epiphyses of the bones. In some cases, genetic testing may be used to confirm the diagnosis.
Treatment[edit]
There is currently no cure for MED. Treatment is focused on managing symptoms and improving quality of life. This may include physical therapy, pain management, and in some cases, surgery to correct bone deformities or replace damaged joints.
See Also[edit]
Ad. Transform your health with W8MD Weight Loss, Sleep & MedSpa

Tired of being overweight?
Affordable GLP-1 weight loss medications
- Semaglutide starting from $29.99/week and up with insurance for visit.
- Tirzepatide starting from $45.00/week and up (dose dependent)
✔ Same-week appointments, evenings & weekends
Learn more:
Start your transformation today with W8MD weight loss centers.
|
WikiMD Medical Encyclopedia |
Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian


