Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes

Fibrodysplasia ossificans progressiva (FOP) is a rare skeletal disorder characterized by congenital malformation of the great toes and progressive heterotopic ossification. Malformation of the great toes appears at birth, while heterotopic ossification generally occurs during childhood and rarely oc...

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Detalles Bibliográficos
Autores principales: Hasegawa, Kosei, Tanaka, Hiroyuki, Futagawa, Natsuko, Miyahara, Hiroyuki, Tsukahara, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436604/
https://www.ncbi.nlm.nih.gov/pubmed/36060212
http://dx.doi.org/10.1155/2022/5021758

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436604/
https://www.ncbi.nlm.nih.gov/pubmed/36060212
http://dx.doi.org/10.1155/2022/5021758

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