Hossain Ibrahim Ageel, Ghadah Mtaen Gosadi and Adeeb Ali Ageel. Unusual Case of Glucose-Galactose Malabsorption with Oculocutaneous Albinism.
. 2017; 5(6):171-173. doi: 10.12691/AJMCR-5-6-10
Glucose-galactose malabsorption, Oculocutaneous albinism, child, Saudi Arabia
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit
[1] | Abdullah AM, el-Mouzan MI, el Shiekh OK, al Mazyad A. Congenital glucose-galactose malabsorption in arab children. J Pediatr Gastroenterol Nutr 1996; 23(5): 561-564. |
|
[2] | Raja M, Kinne RK. Structural insights into genetic variants of Na (+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure. Cell Biochem Biophys 2012; 63(2): 151-158. |
|
[3] | Xin B, Wang H. Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish. Clin Genet 2011; 79(1): 86-91. |
|
[4] | Gracey M, Burke V. Sugar-induced diarrhea in children. Arch Dis Child 1973; 48(5): 331-336. |
|
[5] | Laplane R, Polonovski C, Etiene M, Debray P, Lods JC, Pissarro B. L’intolerance aux sucres a transfert intestinal actif. Arch Fr Pediatr 1962; 19: 895-944. |
|
[6] | Lindquist B, Meeuwisse GW. Chronic diarrhoea caused by monosaccharide malabsorption. Acta Paediatr 1962; 51: 674-685. |
|
[7] | Mutlu M, Cakir M, Aslan Y. Glucose Galactose Malabsorption: A Case Report. HK J Paediatr 2010; 15: 320-323. |
|
[8] | Chdane-Girault C, Dabadie A, Maurage C, Chailloux E, Colin E, Pelatan C, Giniès JL. Neonatal diarrhea due to congenital glucose-galactose malabsorption: report of seven cases. Arch Pediatr 2012; 19(12): 1289-1292. |
|
[9] | Anderson S, Koniaris S, Xin B, Brooks SS. Congenital Glucose-Galactose Malabsorption: A Case Report. J Paediatr health Care 2017; 31(4): 506-510. |
|
[10] | Abdullah AM, Abdullah MA, Abdurrahman MB, al Husain MA. Glucose-galactose malabsorption with renal stones in a Saudi child. Ann Trop Paediatr 1992; 12(3): 327-329. |
|
[11] | Abdullah AM. Aetiology of chronic diarrhea in children: experience at King Khalid University Hospital, Riyadh, Saudi Arabia. Ann Trop Paediatr 1994; 14(2): 111-117. |
|
[12] | Abdullah AM, el-Mouzan MI, el Shiekh OK, al Mazyad A. Congenital glucose-galactose malabsorption in Arab children. J Pediatr Gastroenterol Nutr 1996; 23(5): 561-564. |
|
[13] | El-Naggar W, Balfe JW, Barbar M, Taha D. Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis. Pediatr Nephrol 2005; 20(9): 1336-1339. |
|
[14] | Assiri A, Saeed A, Alnimri A, Ahmed S, Saeed E, Jameel S. Five Arab children with glucose-galactose malabsorption. Paediatr Int Child Health 2013; 33(2): 108-110. |
|
[15] | Ghazali B, Almedhesh SA, Alsuheel AM, Batti D, Shati AA. Congenital glucose-galactose malabsorption: A rare cause of chronic diarrhea. Int J Med Med Sci 2014; 6(2): 59-62. |
|
[16] | Saadah OI, Alghamdi SA, Sindi HH, Alhunaitti H, Bin-Taleb YY, Alhussaini BH. Congenital glucose-galactose malabsorption: A descriptive study of clinical characteristics and outcome from Western Saudi Arabia. Arab J. Gastroenterol. 2014; 15(1): 21-23. |
|
[17] | Al-Baradie RS, Chaudhary MW, Burshaid D, Mir A. Unusual Case of Glucose-Galactose Malabsorption with Infantile Neuroaxonal Dystrophy. Austin J Clin Neurol 2016; 3(2): 1093. |
|
[18] | Berni Canani R, Pezzella V, Amoroso A, et al. Diagnosing and Treating Intolerance to Carbohydrates in Children. Nutrients 2016; 8(3): 157. |
|
[19] | Steinherz R, Nitzan M, Iancu TC. Hypernatremic dehydration as a sign leading to the diagnosis of glucose-galactose malabsorption in breast-fed neonates. Helv Paediatr Acta 1984; 39(3): 275-277. |
|
[20] | Lee WS, Tay CG, Nazrul N, Paed M, Chai PF. A Case of Neonatal Diarrhoea Caused by Congenital Glucose-galactose Malabsorption. Med. J. Malaysia 2009; 64(1): 83-85. |
|
[21] | Vallaeys L, Van Biervliet S, De Bruyn G, Loeys B, Moring AS, Van Deynse E, Cornette L. Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene. Eur J Pediatr 2013; 172(3): 409-411. |
|
[22] | Grønskov K, Ek J, Brondum-Nielsen K. Oculocutaneous albinism. Orphanet J Rare Dis 2007; 2: 43. |
|
[23] | Kamaraj B, Purohit R. Mutational analysis of oculocutaneous albinism: a compact review. Biomed Res Int. 2014; 2014: 905472. |
|
[24] | Khanal S, Pokharel A, Kandel H. Visual deficits in Nepalese patients with oculocutaneous albinism. J Optom. 2016 Apr-Jun; 9(2): 102-109. |
|
[25] | Seward SL Jr, Gahl WA. Hermansky-Pudlak syndrome: health care throughout life. Pediatrics 2013; 132(1): 153-160. |
|