Fibrodysplasia ossificans progressiva · Disease in which fibrous connective tissue turns into bone · YYNN

Fibrodysplasia ossificans progressiva

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Disease in which fibrous connective tissue turns into bone

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Constitutively activated ALK2 and increased SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva.

scientific article published on 06 August 2008

Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva

scientific article

Genetic aspects of fibrodysplasia ossificans progressiva

scientific article

Fibrodysplasia ossificans progressiva

scientific article published on March 2008

Rare form of fibrodysplasia ossificans progressiva

scientific article published on 01 January 1985

Iconographic rubric. Fibrodysplasia ossificans progressiva (myositis ossificans progressiva)

scientific article published on 01 February 1988

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Fibrodysplasia ossificans progressiva (; abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease. Fibrous connective tissue such as muscle, tendons, and ligaments ossify into bone tissue. The condition ultimately immobilises sufferers as new bone replaces...

Instance of

designated intractable/rare disease

class of disease

Signs and symptoms

Subclass of

Connective tissue disease

Genetic disorder

autosomal dominant disease

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