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by Ma, M and Long, Q and Chen, F and Zhang, T and Lu, MS and Wang, WY and Chen, LH
MEDICINE, ISSN 0025-7974, 08/2019, Volume 98, Issue 33, p. e16828
Rationale: Congenital glucose-galactose malabsorption (CGGM) is a rare, autosomal recessive, hereditary disease that usuallypresents in newborns. CGGM... 
MEDICINE, GENERAL & INTERNAL | low-carbohydrate diet | congenital glucose-galactose malabsorption | nutrition management | SLC5A1 | MUTATIONS | free-glucose and galactose formula | Case studies | Birth defects | Diet therapy | Diagnosis | Pediatric research
Journal Article
Journal Article
Journal Article
Gut, ISSN 0017-5749, 08/2019, Volume 68, Issue 11, pp. 2080 - 2091
Lactose is the main source of calories in milk, an essential nutriedigestion, patients with visceral hypersensitivity nt in infancy and a key part of the diet... 
Journal Article
Journal Article
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 02/2018, Volume 66, Issue 2, pp. 250 - 252
ABSTRACTCongenital glucose-galactose malabsorption (cGGM) is a rare autosomal recessive disorder, caused by mutations in the SLC5A1 gene, encoding the... 
Saudi Arabia | mutation | SLC5A1 | congenital glucose-galactose malabsorption | SGLT1 | FAMILY | CHILDREN | NUTRITION & DIETETICS | GENE | CLONING | PEDIATRICS | GASTROENTEROLOGY & HEPATOLOGY | NA+/GLUCOSE COTRANSPORTER | EXPRESSION
Journal Article
Voprosy Detskoi Dietologii, ISSN 1727-5784, 2018, Volume 16, Issue 3, pp. 38 - 42
Journal Article
Clinical Case Reports, ISSN 2050-0904, 01/2019, Volume 7, Issue 1, pp. 51 - 53
Key Clinical Message A three‐day‐old newborn girl presented with decreased feeding and dehydration. She was sick and in shock. She had renal impairment and... 
neonate | glucose‐galactose malabsorption | congenital diarrhea | SLCSA1 gene | glucose-galactose malabsorption | Congenital diseases | Glucose | Mutation | Newborn babies
Journal Article
International Journal of Pediatrics, ISSN 2345-5047, 05/2019, Volume 7, Issue 5, pp. 9399 - 9403
Introduction Glucose-Galactose Malabsorption (GGM) is an autosomal recessive and rare disorder of intestinal transport of glucose and sodium-glucose... 
Diarrhea | case report | Child | Glucose-Galactose Malabsorption
Journal Article
DIGESTIVE DISEASES AND SCIENCES, ISSN 0163-2116, 01/2017, Volume 62, Issue 1, pp. 280 - 281
Journal Article
HORMONE RESEARCH IN PAEDIATRICS, ISSN 1663-2818, 2017, Volume 87, Issue 4, pp. 277 - 282
Background/Aims: Glucose-galactose malabsorption (GGM) is a rare and potentially fatal disorder. The autosomal recessive mutation of the SGLT1 gene interferes... 
VITAMIN-D | Glucose-galactose malabsorption | Nephrocalcinosis | SGLT1 | CA(V)1.3 | CHILDREN | Hypercalcemia | CALCIUM-ABSORPTION | TRANSPORT | TRPV6 | ENDOCRINOLOGY & METABOLISM | INTESTINAL GLUCOSE | PEDIATRICS | ASSOCIATION
Journal Article
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