Connective tissue presentation in two families expands the phenotypic spectrum of PYROXD1 disorders

Recessive variants in the oxidoreductase PYROXD1 are reported to cause a myopathy in 22 affected individuals from 15 families. Here, we describe two female probands from unrelated families presenting with features of a congenital connective tissue disorder including osteopenia, blue sclera, soft ski...

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Detalles Bibliográficos
Autores principales: Evesson, Frances J, Dziaduch, Gregory, Bryen, Samantha J, Moore, Francesca, Pittman, Sara, Devanapalli, Beena, Waddell, Leigh B, Ryan, Monique M, Menezes, Manoj P, Weihl, Conrad C, Tolun, Adviye Ayper, Zaidman, Craig, Young, Helen, Adès, Lesley C, Cooper, Sandra T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244218/
https://www.ncbi.nlm.nih.gov/pubmed/36920481
http://dx.doi.org/10.1093/hmg/ddad035

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244218/
https://www.ncbi.nlm.nih.gov/pubmed/36920481
http://dx.doi.org/10.1093/hmg/ddad035

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