Article

Congenital Malformation of The Great Toe in Children. Did You Exclude Fibrodysplasia Ossificans Progressiva – FOP.

2021-10-18

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and severely disabling genetic disorder. The worldwide prevalence is approximately 1 per 2 million. Heterozygous mutations in ACVR1/ALK2 gene exist in all sporadic and familial cases of FOP. The primary aim of this study is to describe the clinical course of three children suffering from FOP and follow...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 404663bc-fbf3-55d6-9d39-4b1fbb038ce2
DOI: 10.21203/rs.3.rs-963656/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Congenital Malformation of The Great Toe in Children. Did You Exclude Fibrodysplasia Ossificans Progressiva – FOP.DOI 10.21203/rs.3.rs-963656/v1Read

Pay Attention to the Osteochondromas in Fibrodysplasia Ossificans Progressiva.Semantic proximity Read

Fibrodysplasia ossificans progressiva (FOP): watch the great toes!Semantic proximity Read

The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call.Semantic proximity Read

Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.Semantic proximity Read

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report.Semantic proximity Read

Nonclassic fibrodysplasia ossificans progressiva: A child from Angola with an ACVR1G328E variant.Semantic proximity Read

[Recommendations for the healthcare of patients with FOP].Semantic proximity Read

Fibrodysplasia ossificans progressiva: clinical and genetic aspects.Semantic proximity Read

My Phenotype speaks: please do not harm me with biopsy needle.Semantic proximity Read

Fibrodysplasia Ossificans Progressiva.Semantic proximity Read

Challenges in the diagnosis of fibrodysplasia ossificans progressiva with the ACVR1 mutation (c.774G > C, p.R258S): a case report and review of literature.Semantic proximity Read

ACVR1 (587T>C) mutation in a variant form of fibrodysplasia ossificans progressiva: second report.Semantic proximity Read