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An Essential Parameters of Hereditary Fructose Intolerance Include Etiology, Epidemiology, Patho Physiology, Histo Pathology, Diagnosis, Differential Diagnosis, Treatment and Prognosis

Year: 2026

Type: article

Abstract: Patients with hereditary fructose intolerance, an autosomal recessive condition, do not have the enzyme necessary to break down fructose-1-phosphate. This illness typically manifests as nausea, vomiting, jaundice, and hypoglycemia during the weaning phase. Early detection is crucial, as is the quick implementation of dietary restrictions to reduce fructose.The evaluation and treatment of patients with genetic fructose intolerance are discussed in this activity, which also emphasizes the importance of an interdisciplinary team in the treatment of such patients.

Source: Zenodo (CERN European Organization for Nuclear Research)

DOI: 10.5281/zenodo.19229586

Authors: Muralinath E., Guruprasad M., Madhavi Latha C., Sheethal U., Vyshnavi J., Varsha V., Prathysha M.V.S., Karthik Jayanyj Y.

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W7140703170

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