Ataxia
Description | Basic evaluations: CRP, blood count, urine status Additional evaluations for etiological investigations: In children metabolic screening in the urine (amino acids, organic acids, urea-cycle-defects), serum-liquor-diagnostics (+ cells, + glucose, + lactate, + oligoclonal immunoglobuline), HSV, CMV, EBV, syphilis, borrelia, mycobacteria, ANA, ENA, further auto-antibodies, immune-fixation, very long chain fatty acids (VLCFA), phytanic acid, AFP, IgA, IgE, cholesterol, HDL, LDL, triglycerides, ammoniac, copper, coeruloplasmin, lactate, hexosaminidase A & B, arylsulfatase A, vitamin B1, vitamin E, vitamin B12, methylmalonic acid, folic acid Friedreich’s ataxia: Evaluation of the amount of GAA-trinucleotides with PCR. Genetic consultation required. Teleangiectasic ataxia: Molecular-genetic evaluation possible. Spinocerebellar ataxia: Molecular-genetic evaluation possible. |
More Results for the letter A
- AB0-incompatibility
- Abdomen, acute or chronic pains
- Abortion
- Abortion (early abortion, before the 16th week of pregnancy)
- Abortion, habitual (minimum of three consecutive abortions)
- Acanthosis nigricans
- Achondroplasia
- Acne
- Acrocyanosis
- Acrodermatitis chronica atrophicans
- Acromegaly
- Acute abdomen
- Acute disseminated encephalomyelitis (ADEM)
- Acute leukemia
- Addison, M.
- Adenomatous polyposis coli
- Adipositas
- Adnexitis
- Adrenogenital syndrome (congenital adrenal hyperplasia)
- Adrenoleucodystrophy
- Agranulocytosis
- AGS
- Alcaptonuria
- Alcoholism
- Alkaline phosphatase increase
- Allergic granulomatous arteritis
- Allergy diagnostics
- Alopecia
- Alport’s syndrome
- ALS