Severe Hepatitis: An Unusual Presentation of Phosphomannomutase 2 Deficiency
Phosphomannomutase 2 deficiency congenital disorder of glycosylation (PMM2-CDG), the most prevalent N-glycosylation disease, is a multi-organ disease with marked clinical heterogeneity. Severe liver involvement is not a common find in these patients. A six-month-old girl was referred to the emergen...
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Autores principales: | Catarina Pinto Silva, Joana Almeida, Luísa Diogo, Susana Nobre |
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Formato: | article |
Lenguaje: | EN PT |
Publicado: |
Sociedade Portuguesa de Pediatria
2021
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Acceso en línea: | https://doaj.org/article/a8e59ae98ab040ada7075743f71c2eba |
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