Asymptomatic parental mosaicism for osteogenesis imperfecta associated with a new splice site mutation in COL1A2

Recurrent lethal perinatal osteogenesis imperfecta may result from asymptomatic parental mosaicism. A previously unreported mutation in COL1A2 leads to recurrent cases of fetal osteogenesis imperfecta Sillence type IIA, which emphasizes the importance of clinical and genetic evaluation of mosaicism...

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Detalles Bibliográficos
Autores principales: Frederiksen, Anja Lisbeth, Duno, Morten, Johnsen, Iben B. G., Nielsen, Morten Frost, Krøigård, Anne Bruun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054473/
https://www.ncbi.nlm.nih.gov/pubmed/27761249
http://dx.doi.org/10.1002/ccr3.658

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054473/
https://www.ncbi.nlm.nih.gov/pubmed/27761249
http://dx.doi.org/10.1002/ccr3.658

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