Malabsorption

Author(s):  
Satish Keshav ◽  
Alexandra Kent

Malabsorption is defined as a defect in the digestion and absorption of nutrients by the gastrointestinal tract. It can lead to a specific nutritional deficiency (‘selective’ malabsorption, such as vitamin B12 deficiency) or a general nutritional deficiency (global malabsorption, such as that due to diseases affecting the mucosa diffusely, such as Crohn’s disease). The commonest causes of malabsorption are coeliac disease and pancreatic exocrine insufficiency.


2013 ◽  
Vol 7 ◽  
pp. S68
Author(s):  
M. Ward ◽  
V. Kariyawasam ◽  
A. Sobczynska-Malefora ◽  
A. Ajaegbu ◽  
J. Sanderson ◽  
...  


Gut ◽  
2013 ◽  
Vol 62 (Suppl 1) ◽  
pp. A168.2-A168
Author(s):  
M G Ward ◽  
V C Kariyawasam ◽  
P A Blaker ◽  
K V Patel ◽  
R M Goel ◽  
...  


2009 ◽  
Vol 136 (5) ◽  
pp. A-177-A-178
Author(s):  
Santiago García López ◽  
Sonia Gallego Montañes ◽  
Fernando Gomollon ◽  
Marta Gracia Ruiz ◽  
Raquel Vicente Lidón


2017 ◽  
Vol 42 (1) ◽  
pp. 25-27
Author(s):  
Joo-Hee Lee ◽  
Youn-Jung Park ◽  
Jeong-Seung Kwon ◽  
Young-Gun Kim ◽  
Hyung-Joon Ahn


2017 ◽  
Vol 35 (5) ◽  
pp. 463-471
Author(s):  
Shuzi Zheng ◽  
Chaoqun Wu ◽  
Wei Yang ◽  
Xuanping Xia ◽  
Xiuqing Lin ◽  
...  

Objectives: The study aimed to investigate the association of Crohn's disease (CD) with transcobalamin II (TCN2) polymorphisms and serum homocysteine, folate, and vitamin B12 levels. Methods:TCN2 (rs1801198, rs9606756) were genotyped by iMLDR in 389 CD patients and 746 controls. Furthermore, 102 CD patients and 153 controls were randomly selected for examination of serum homocysteine, folate, and vitamin B12 levels by enzymatic cycling assay and chemiluminescence immunoassay, respectively. Results: Mutant allele (G) and genotype (AG + GG) of (rs9606756) were higher in CD patients than in controls (both p < 0.05). So were they in ileocolonic CD patients and stricturing CD patients compared to controls (all p < 0.05). Mutant allele (G) and genotype (CG + GG) of (rs1801198) were more prevalent in stricturing CD patients than in controls (both p < 0.05). Compared to controls, average homocysteine level was enhanced in CD patients (p = 0.003), whereas average folate and vitamin B12 levels were reduced in CD patients (both p < 0.001). The prevalence of hyperhomocysteinemia, folate deficiency, and vitamin B12 deficiency was higher in CD patients than in controls (all p < 0.01). Both folate deficiency and vitamin B12 deficiency were independently related to risk of CD (both p < 0.01). Conclusion:TCN2 (rs1801198, rs9606756) polymorphisms as well as folate deficiency and vitamin B12 deficiency are correlated with CD.



Author(s):  
Atsuko FUKAZAWA ◽  
Toshio NAKAMURA ◽  
Keiji MARUYAMA ◽  
Sigeo MIYAZAKI ◽  
Satoshi NAKAMURA


Blood ◽  
1966 ◽  
Vol 28 (5) ◽  
pp. 770-775 ◽  
Author(s):  
E. J. WATSON-WILLIAMS ◽  
A. F. FLEMING

Abstract A Nigerian patient is described with megaloblastic anemia due to vitamin B12 deficiency. The deficiency resulted from malabsorption of the vitamin, but no other abnormal functioning of the gastrointestinal tract could be demonstrated. The patient did not have addisonian pernicious anemia. He had remarkable hyperpigmentation of the skin, especially of the palms of the hands. What is known of possible connections between megaloblastic anemias and melanin metabolism cannot explain this hyperpigmentation.



Nutrients ◽  
2017 ◽  
Vol 9 (3) ◽  
pp. 308 ◽  
Author(s):  
Fernando Gomollón ◽  
Carla Gargallo ◽  
Jose Muñoz ◽  
Raquel Vicente ◽  
Alberto Lue ◽  
...  


1977 ◽  
Vol 55 (12) ◽  
pp. 595-601 ◽  
Author(s):  
H. C. Heinrich ◽  
E. E. Gabbe ◽  
H. Bartels ◽  
K. H. Oppitz ◽  
Ch Bender-G�tze ◽  
...  


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