Lactose intolerance
Description | There are three different methods to determine lactose intolerance:
Genetic evidence of lactase-gene-polymorphism. In the FRG, the CC- or CT-polymorphisms with accompanying lactose-intolerance-predisposition are evident in 15-25% of the normal population. The existence of those variants does not necessarily lead to clinical symptoms of lactose intolerance.
This is a functional test, which enables evidence of hereditary as well as acquired types of lactose-intolerance and is carried out in our laboratory practice (duration approximately 3 hours). Please see function tests.
This is also a functional test. After administering 50 g lactose there will be multiple blood extractions for evaluation of glucose. Please refer to function tests.
Addendum: On clinical suspicion of lactose-intolerance in children, an additional stool testing for lamblia is recommended. |
More Results for the letter L
- Lactose intolerance
- Lambert-Eaton-myasthenia-syndrome (LEMS)
- Laryngitis, tracheitis, pseudocroup
- Lead intoxication:
- Leukemia, acute
- Leukemia, chronic myeloid
- Leukocytosis
- Leukopenia
- Lichen planus
- Limbic encephalitis
- Lipometabolic disorder
- Liquorrhea
- Livedo racemosa
- Liver carcinoma
- Liver cirrhosis
- Liver parenchyma damage
- Low libido, male
- LUF (Luteinized unruptured follicle syndrome)
- Lung emphysema (before the age of 50)
- Lung sarcoidosis
- Lung-carcinoma
- Lupus erythematosus, systemic (SLE)
- Lymphadenopathy
- Lymphocytosis (> 4000/µl)
- Lymphogranuloma venereum
- Lymphoma
- Lymphopenia (< 1000/µl)
- Lymphotropic pathogens