Fructosuria
A benign hereditary defect of FRUCTOSE metabolism that results in a sharp increase in fructose excretion in the urine following ingestion of dietary fructose, SUCROSE, or SORBITOL. It is caused by mutations in the ketohexokinase (KHK) gene. OMIM: 229800
Also Known As:
Essential benign fructosuria; Hepatic fructokinase deficiency; Ketohexokinase deficiency
Networked: 25
relevant articles (0 outcomes,
1 trials/studies)
Bio-Agent Context: Research Results
Experts
1. | González-Devia, Deyanira:
1 article
(01/2019)
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2. | Lemus, Hernan Nicolas:
1 article
(01/2019)
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3. | Mendivil, Carlos O:
1 article
(01/2019)
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4. | Morales-Alvarez, Martha Catalina:
1 article
(01/2019)
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5. | Ricardo-Silgado, Maria Laura:
1 article
(01/2019)
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6. | Akiyama, Taro E:
1 article
(01/2018)
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7. | Askew, Roger:
1 article
(01/2018)
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8. | Cao, Jin:
1 article
(01/2018)
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9. | Herath, Kithsiri:
1 article
(01/2018)
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10. | Li, Cai:
1 article
(01/2018)
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