Mathews Journal of Gastroenterology & Hepatology

2572-6471

Previous Issues Volume 10, Issue 2 - 2025

The Clinical Picture of Galactosemia Can Manifest Itself with Varying Intensity

Siniša Franjić*

Independent Researcher, Croatia

*Corresponding author: Siniša Franjić, Independent Researcher, Croatia; Email: [email protected]

Received Date: June 11, 2025

Published Date: July 08, 2025

Citation: Franjić S. (2025). The Clinical Picture of Galactosemia Can Manifest Itself with Varying Intensity. Mathews J Gastroenterol Hepatol. 10(2):34.

Copyrights: Franjić S. © (2025).

ABSTRACT

Galactosemia is a rare hereditary metabolic disorder that influences a person's ability to properly metabolize galactose. Galactosemia has an autosomal recessive inheritance design that comes about in a lack of the chemical dependable for the appropriate breakdown of galactose. The clinical picture can show itself with shifting concentrated. In a normal frame, side effects show up 2-3 days after drain ingestion with heaving, expanded jaundice, diarrhea, flatulence, abdominal distension due to liver enlargement, dehydration, symptoms of hypoglycemia, and a exceptionally poor general condition.

Keywords: Galactosemia, GALT, Galactose, Pathology, Health.


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