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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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| Publicado en: | Case Rep Hematol |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Hindawi Publishing Corporation
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5149635/ https://ncbi.nlm.nih.gov/pubmed/28018685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/1351873 |
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