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
- Alveolitis, exogenous allergic
- Alzheimer’s dementia
- Amalgam
- Amebiasis
- Amenorrhea
- Amyloidosis:
- Amyotrophic lateral sclerosis (ALS)
- Anabolic intake
- Analgesic-related nephropathy
- Anaphylactic shock
- Ancylosing spondylitis (Bechterew’s disease)
- Androgen-deficiency in men
- Androgenisation phenomena
- Anemia-diagnostics
- Angina pectoris
- Angio-neurotic edema
- Ankylosing spondylitis
- Anorexia nervosa
- Anovulation
- Anti-coagulants therapy
- Anti-convulsants (Initial drug regimen / therapy monitoring)
- Anti-epileptics
- Anti-NMDA-receptor-encephalitis
- Anti-phospholipid syndrome
- Anti-synthetase syndrome
- Antibody insufficiency
- Antioxidants
- Anuria
- Aphthen
- Aplastic anemia