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Different Presentations of Patients with Transcobalamin II Deficiency: A Single-Center Experience from Turkey
OBJECTIVE: Transcobalamin II deficiency is a rare autosomal recessive disease characterized by decreased cobalamin availability, which in turn causes accumulation of homocysteine and methylmalonic acid. The presenting clinical features are failure to thrive, diarrhea, megaloblastic anemia, pancytope...
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| Publicado no: | Turk J Haematol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Galenos Publishing
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6373502/ https://ncbi.nlm.nih.gov/pubmed/30185401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjh.galenos.2018.2018.0230 |
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