Glucose-Galactose Malabsorption: Causes, Symptoms, …
2024年7月10日 · Glucose-galactose malabsorption (GGM) is a very rare inherited genetic condition, with only approximately 300 cases worldwide. GGM is also sometimes known as SGLT1 deficiency. This is because a...
Glucose-galactose malabsorption - MedlinePlus
Glucose-galactose malabsorption is a condition in which the body cannot take in (absorb) the sugars glucose and galactose, which primarily results in severe diarrhea. Explore symptoms, inheritance, genetics of this condition.
Glucose-galactose malabsorption - Wikipedia
Glucose-galactose malabsorption is a rare condition in which the cells lining the intestine cannot take in the sugars glucose and galactose, which prevents proper digestion of these molecules and larger molecules made from them. Glucose and galactose are called simple sugars, or monosaccharides.
Glucose-Galactose Malabsorption - Symptoms, Causes, …
2020年8月10日 · Glucose-galactose malabsorption (GGM) is an inherited metabolic disorder. It is caused by the small intestines not being able to absorb and use glucose and galactose (simple sugars). Glucose and galactose have very similar chemical structures.
Glucose-galactose malabsorption | About the Disease | GARD
Glucose-galactose malabsorption (GGM) is a genetic condition in which the sugars glucose and galactose cannot be properly absorbed by the body. Infants with GGM develop severe diarrhea resulting in severe dehydration, acidosis, and weight loss in the first few weeks of life.
Glucose Galactose Malabsorption (GGM) - Boston Children's Hospital
Glucose galactose malabsorption causes symptoms when a child ingests the sugars glucose or galactose. The primary symptom is severe diarrhea, which can lead to dehydration and weight loss that may become life threatening.
Glucose-galactose malabsorption: Causes and treatments - Medical News Today
2024年3月7日 · Glucose-galactose malabsorption (GGM) is a rare metabolic condition. It occurs when a genetic variation makes the body unable to properly absorb the simple sugars glucose and galactose.
glucose-galactose malabsorption
Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period.
Orphanet: Glucose-galactose malabsorption
A rare, potentially lethal, autosomal recessive metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset in the neonatal period.
Glucose-Galactose Malabsorption - Metabolic Support UK
It is involved in the process of using energy to move glucose and galactose across the cell membrane for absorption. Mutation in the SLC5A1 gene, prevents the SGLT1 protein from performing its function which leads to a build up of glucose and galactose in the intestinal tract.
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