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Congenital intestinal transport defect
- ... apolipoprotein B-like protein in intestinal cells Lipid transport defect of intestine Genetic Testing Registry: Chylomicron retention disease Chylomicron retention ...
- ... of the condition. Congenital defect of folate absorption Congenital folate malabsorption Folic acid transport defect Genetic Testing Registry: Congenital defect of folate absorption ...
- ... chest cavity (the diaphragm), which is called a congenital diaphragmatic hernia. This potentially serious birth defect allows the stomach and intestines to move into the chest and possibly crowd ...
- ... the chest cavity (the diaphragm). The most common defect is a congenital diaphragmatic hernia, which is a hole in the diaphragm that develops before birth. This hole allows the stomach and intestines to move into the chest and crowd the ...
- Lymphedema (Lymphatic Education & Research Network)Lymphedema/Start Here ... Lymphedema ... Lymphatic Education & Research Network ... lymphedema, lymphatic system, risk of lymphedema, treatment for lymphedema ... Lymphedema ...
- ... history of the disorder in their family. Copper transport disease Hypocupremia, congenital Kinky hair syndrome Menkea syndrome Menkes disease MK ...
- ... R, Grosso S, Gartner J. Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed ...
- ... them. During the digestion of food, the protein transports the sugars into the cells that line the wall of the intestine (intestinal epithelial cells) as food passes through.The ...
- ... SGLT1). This protein is found mainly in the intestinal tract and the kidneys. It spans the membrane of cells and moves (transports) two sugars called glucose and galactose from outside ...
- Anemia/Start Here ... Anemia ... National Heart, Lung, and Blood Institute ... YOUR GUIDE TO ANEMIA, prevent, treat, control. ... PDF ... From the National Institutes of Health