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Fibrodysplasia ossificans progressiva: from clinical complexity to therapeutic opportunity

Abstract Fibrodysplasia Ossificans Progressiva (FOP) is an ultra-rare and severely disabling genetic disorder affecting approximately one in two million individuals worldwide. It is characterised by progressive endochondral heterotopic ossification (HO), in which ectopic cartilage formation precedes...

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Hoofdauteurs: Amrita Chakraborty, Uday Sankar Chakrabarty, Mainak Mal, Susanta Paul, Dibya Sinha, Arvind Kumar, Nilanjan Sarkar
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer 2026-01-01
Reeks:Journal of Rare Diseases
Onderwerpen:
Fibrodysplasia ossificans progressiva
Heterotopic ossification
ACVR1 mutation
Gene and targeted therapies
Online toegang:https://doi.org/10.1007/s44162-025-00144-4
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