An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case report

BACKGROUND: Hereditary folate malabsorption—a rare disorder caused by impairment of the folate transporter—can develop into severe folate deficiency manifesting as megaloblastic anemia and occasionally thrombocytopenia. Reportedly, megaloblastic anemia can manifest with hemorrhagic episodes, possibl...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakurai, Yukari, Toriumi, Naohisa, Sarashina, Takeo, Ishioka, Toru, Nagata, Marino, Kobayashi, Hiroya, Azuma, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245286/
https://www.ncbi.nlm.nih.gov/pubmed/35773682
http://dx.doi.org/10.1186/s13256-022-03448-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245286/
https://www.ncbi.nlm.nih.gov/pubmed/35773682
http://dx.doi.org/10.1186/s13256-022-03448-x

Ejemplares similares