Loading

Corpus Journal of Clinical Trials
[ ISSN : 2833-3764 ]


Galactosemia a Disease that you Need to know

Review Article
Volume 3 - Issue 1 | Article DOI : 10.54026/CJCT/1010


Yolanda Cifuentes C1*, Sergio Mateus B2

1Department of Pediatrics, Division of Neonatology, Universidad Nacional de Colombia
2Neonatologist, Universidad Nacional de Colombia

Corresponding Authors

Yolanda Cifuentes C, Neonatologist, Universidad Nacional de Colombia

Keywords

Galactosemia; Inborn Error of Metabolism; Newborn Jaundice

Received : September 07, 2022
Published : September 20, 2022

Abstract

Galactosemia is an autosomal recessive disease, caused by the deficit of any of the four enzymes involved in the metabolism of galactose, derived from the disaccharide lactose, on its way to becoming glucose. Knowledge of this pathology and a high index of suspicion will allow early diagnosis and treatment, thus decreasing the associated complications and even mortality. We will present a brief summary of the disease in the context of a patient treated in our neonatology service.