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  2. Multiple epiphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_epiphyseal_dysplasia

    Multiple epiphyseal dysplasia (MED), also known as Fairbank's disease, is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the growing ends of bones. Long bones normally elongate by expansion of cartilage in the growth plate (epiphyseal plate) near their ends.

  3. Femoral head ostectomy - Wikipedia

    en.wikipedia.org/wiki/Femoral_head_ostectomy

    It may be used in some cases of hip dysplasia, an extremely painful congenital condition found in many dog breeds and some cats. [4] It is also performed in cases of trauma where the head of the femur is badly broken or severed, or in response to other diseases of the hip bone, such as Legg-Calve-Perthes' disease .

  4. Autosomal recessive multiple epiphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Autosomal_recessive...

    Autosomal recessive multiple epiphyseal dysplasia (ARMED), also called epiphyseal dysplasia, multiple, 4 (EDM4), multiple epiphyseal dysplasia with clubfoot or –with bilayered patellae, [1] is an autosomal recessive [2] congenital disorder affecting cartilage and bone development.

  5. List of dog diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_dog_diseases

    Treatment options include medications such as NSAIDs, corticosteroids, and joint fluid modifiers such as glycosaminoglycans. Other treatments include surgery, massage, warm compresses, chiropractic, and acupuncture. [35] Hip dysplasia is an inherited disease in dogs that is characterized by abnormal development of the acetabulum and head of the ...

  6. Spondyloepiphyseal dysplasia congenita - Wikipedia

    en.wikipedia.org/wiki/Spondyloepiphyseal...

    X-ray of the spine in a patient with spondyloepimetaphyseal dysplasia. Spondyloepiphyseal dysplasia congenita is one of a spectrum of skeletal disorders caused by mutations in the COL2A1 gene. [3] The protein made by this gene forms type II collagen, a molecule found mostly in cartilage and in the clear gel that fills the eyeball (the vitreous).

  7. Wolcott–Rallison syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolcott–Rallison_syndrome

    The other features include multiple epiphyseal dysplasia, osteopenia, intellectual disability, and hepatic and renal dysfunction. [1] Patients having features that suggest Wolcott–Rallison syndrome can be referred for genetics testing. The key way to test for this disease is through genetic testing for EIKF2AK3 mutations. [7]