glucose-galactose malabsorption

glucose-galactose malabsorption: an autosomal recessive disorder caused by mutation in the SLC5A1 (SGLT1) gene (locus: 22q13.1), which encodes the intestinal sodium/glucose cotransporter, resulting in defective intestinal glucose and galactose transport. It is characterized by neonatal onset of profuse, acidic, watery diarrhea leading to severe dehydration and death if untreated; it can be treated by a glucose- and galactose-free diet.

Игры ⚽ Нужно решить контрольную?

Glucose-galactose malabsorption — Classification and external resources ICD 10 E74.3 ICD 9 271.3 … Wikipedia
Galactose-1-phosphate uridylyltransferase deficiency — Classification and external resources Galactose ICD 10 E … Wikipedia
Fructose malabsorption — Classification and external resources Fructose ICD 10 E … Wikipedia
Natrium/Glucose-Cotransporter 1 — Masse/Länge Primärstruktur 664 Aminosäuren … Deutsch Wikipedia
Sodium-glucose transport proteins — solute carrier family 5 (sodium/glucose cotransporter), member 1 Identifiers Symbol SLC5A1 Alt. symbols SGLT1 Entrez … Wikipedia
malabsorption — Imperfect, inadequate, or otherwise disordered gastrointestinal absorption. congenital selective glucose and galactose m. an inherited disorder in which d glucose and d galactose accumulate in the intestinal lumen and exert an osmotic … Medical dictionary
GGM — glucose galactose malabsorption … Medical dictionary
GGM — • glucose galactose malabsorption … Dictionary of medical acronyms & abbreviations
SLC5A1 — Solute carrier family 5 (sodium/glucose cotransporter), member 1, also known as SLC5A1, is a human gene.cite web | title = Entrez Gene: SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1| url =… … Wikipedia
Galactosemia — Classification and external resources Galactose ICD 10 E … Wikipedia

Academic Dictionaries and Encyclopedias