Clinical heterogeneity in congenital sucrase-isomaltase deficiency

Journal of Pediatrics

Volumn 128, Issue 6, 1996, Pages 727-729

  Treem, W R ^a  

^a DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; OLIGO 1,6 GLUCOSIDASE; SUCRASE ISOMALTASE;

BRUSH BORDER; CHRONIC DIARRHEA; ENZYME ACTIVITY; ENZYME DEFICIENCY; GLUCOSE METABOLISM; HUMAN; NOTE; PRIORITY JOURNAL;

EID: 0029898558     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(96)70320-7     Document Type: Editorial

References (15)

1. T Newton MS Murphy IW Booth Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency J Pediatr 128 1996 753 756
2. JJ Kelly DH Alpers Properties of human intestinal glucoamylase Biochem Biophys Acta 315 1973 113 120
3. WR Treem Congenital sucrase-isomaltase deficiency J Pediatr Gastroenterol Nutr 21 1995 1 14
4. R Ringrose H Preiser JD Welsh Sucrase-isomaltase (palatinasc) deficiency diagnosed during adulthood Dig Dis Sci 25 1980 384 387
5. EE Sterchi MJ Lentze HY Naim Molecular aspects of disaccharidase deficiencies Baillieres Clin Gastroenterol 4 1990 79 96
6. JAM Fransen HP Hauri LA Ginsel HY Naim Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for existence of an intracellular sorting signal in the isomaltase subunit J Cell Biol 115 1991 45 57
7. WR Treem N Ahsan B Sullivan Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency Gastroenterology 105 1993 1061 1068
8. H Skovbjerg PA Krasilnikoff Maltase-glucoamylase and residual isomaltase in sucrose-intolerant patients J Pediatr Gastroenterol Nutr 5 1986 365 371
9. E Lebenthal PC Lee Glucoamylase and disaccharidase activities in normal subjects and in patients with mucosal injury of the small intestine J Pediatr 97 1980 389 393
10. H Skovbjerg Immunoelectrophoretic studies of human small intestinal brush border proteins: the longitudinal distribution of peptidases and disaccharidases Clin Chem Acta 112 1981 205 212
11. E Eggermont HG Hers The sedimentation properties of the intestinal α-glucosidases of normal human subjects and of patients with sucrose intolerance Eur J Biochem 9 1969 488 496
12. E Lebenthal K Maung-U BY Zheng Small intestinal glucoamylase deficiency and starch malabsorption: a newly recognized α-glucosidase deficiency in children J Pediatr 124 1994 541 546
13. B Hadorn JR Green EE Sterchi Biochemical mechanisms in congenital enzyme deficiencies of small intestine Clin Gastroenterol 10 1981 671 690
14. H Hinrich-Karsten RM Bertele-Harms D Bruer-Kleis Enzyme-substitution therapy with the yeast saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency N Engl J Med 316 1987 1306 1309
15. RH Yolken W Hart I Oung Gastrointestinal dysfunction and disaccharide intolerance in children infected with human immunodeficiency virus J Pediatr 118 1991 359 363