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Neurological involvement in hereditary transcobalamin II deficiency.
A case of hereditary transcobalamin II deficiency with neurological involvement is described. The patient presented in early infancy with megaloblastic anaemia and was treated with folinic acid from 6 weeks of age. The diagnosis of transcobalamin II deficiency was not made until he was 2 years old w...
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| Publicado no: | J Neurol Neurosurg Psychiatry |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1982
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC491269/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7062075/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.45.1.74 |
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