Expanding the phenotypic spectrum of osteogenesis imperfecta type V including heterotopic ossification of muscle origins and attachments

BACKGROUND: Osteogenesis imperfecta (OI) is a clinical and genetic heterogeneous group of connective tissue disorders, characterized by bone fragility and a propensity to fracture. METHODS: In this report we describe the clinical phenotype of two patients, a 28‐year‐old woman and her mother (54 year...

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Detalles Bibliográficos
Autores principales: Clewemar, Pantelis, Hailer, Nils P., Hailer, Yasmin, Klar, Joakim, Kindmark, Andreas, Ljunggren, Östen, Stattin, Eva‐Lena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625150/
https://www.ncbi.nlm.nih.gov/pubmed/31099171
http://dx.doi.org/10.1002/mgg3.723

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625150/
https://www.ncbi.nlm.nih.gov/pubmed/31099171
http://dx.doi.org/10.1002/mgg3.723

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