Cargando…
SGLT2 inhibition alleviated hyperglycemia, glucose intolerance, and dumping syndrome-like symptoms in a patient with glycogen storage disease type Ia: a case report
BACKGROUND: Glycogen storage disease (GSD) type Ia is a glycogenesis disorder with long-term complications such as hepatomegaly and renal dysfunction and is caused by congenital loss of glucose-6-phosphatase (G6Pase) expression. G6Pase is essential for the final step of gluconeogenesis and glycogeno...
Autores principales: | Katayama, Daisuke, Baba, Hiroo, Kuwabara, Takashige, Kido, Jun, Mitsubuchi, Hiroshi, Matsumoto, Shirou, Nakamura, Kimitoshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885476/ https://www.ncbi.nlm.nih.gov/pubmed/33588940 http://dx.doi.org/10.1186/s13256-020-02658-5 |
Ejemplares similares
-
Clinical manifestations in two patients with pyruvate dehydrogenase deficiency and long-term survival
por: Yoshida, Takanobu, et al.
Publicado: (2017) -
Biochemical and clinical features of hereditary hyperprolinemia
por: Mitsubuchi, Hiroshi, et al.
Publicado: (2014) -
Hyperammonemia crisis following parturition in a female patient with ornithine transcarbamylase deficiency
por: Kido, Jun, et al.
Publicado: (2017) -
Caracteristiques de ia cible "dump" 47
por: Potier, J.P
Publicado: (1970) -
Carglumic Acid Contributes to a Favorable Clinical Course in a Case of Severe Propionic Acidemia
por: Kido, Jun, et al.
Publicado: (2020)