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Severe pancytopenia at the presentation of Imerslund-Gräsbeck syndrome in a 23-month-old Italian boy

Abstract Background Imerslund-Gräsbeck syndrome (IGS) is a rare autosomal recessive disorder characterized by megaloblastic anemia due to selective cobalamin malabsorption and benign proteinuria. IGS is caused by a disfunction of the cubam receptor, which mediates the reabsorption of cobalamin in th...

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Bibliografische gegevens
Hoofdauteurs: Francesca Di Sario, Francesca Piloni, Francesco Gasparini, Eleonora Serpetti, Barbara Bruschi, Paola Coccia, Maria Elena Lionetti, Simona Gatti
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMC 2024-09-01
Reeks:Italian Journal of Pediatrics
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Online toegang:https://doi.org/10.1186/s13052-024-01759-x
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