Coexistence of Factor VII Deficiency and Hereditary Spastic Paraplegia in Two Siblings

We present the case of two patients aged 12 years and 7 years who were referred to our hospital for factor VII deficiency inherited in an autosomal recessive pattern, who had suffered from previous multiple joint haemarthroses. They presented with fine motor symptoms and difficulty in walking. Durin...

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Detalles Bibliográficos
Autores principales: De la Corte-Rodriguez, Hortensia, Rodriguez-Merchan, E. Carlos, Alvarez-Roman, M. Teresa, Hernandez-Moreno, Ana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5149635/
https://www.ncbi.nlm.nih.gov/pubmed/28018685
http://dx.doi.org/10.1155/2016/1351873

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5149635/
https://www.ncbi.nlm.nih.gov/pubmed/28018685
http://dx.doi.org/10.1155/2016/1351873

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