Fibrodysplasia ossificans progressiva

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Myositis ossificans progressiva (Fibrodysplasia ossificans progressiva)

1967
Unter den wechselnden Bezeichnungen fur die pathologische Verknocherung von Muskeln, Sehnen und Bandern verbirgt sich ein einheitliches Krankheitsbild, dessen erbliche Wurzel nicht zu ubersehen ist. Das Wesen der Erkrankung wird durch die gebrauchlichen Synonyma nur umschrieben: Myositis ossificans progressiva, Exostosis luxurians ...
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Fibrodysplasia ossificans progressiva in China

Bone, 2018
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and devastating disorder characterized by cumulative episodes of progressive heterotopic ossification. It is estimated that there exist 600-700 patients in Mainland China. Nevertheless, due to the rarity, many FOP patients were initially misdiagnosed.
Dunmin, She, Keqin, Zhang
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Fibrodysplasia ossificans progressiva.

European journal of dermatology : EJD, 2003
Fibrodysplasia ossificans progressiva, a rare genetic disabling disease characterized by heterotopic bone formation, is of special interest for general medicine since the bone morphogenetic proteins (especially BMP-4) involved in its pathogenesis are known to play a role in skeletal morphogenesis, and the gene antagonist to BMP-4 noggin might be useful
Maria, Blaszczyk +3 more
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Fibrodysplasia ossificans progressiva