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
- Appendicitis
- Appetite, loss of
- Apudoma
- ARDS (acute respiratory distress syndrome)
- Arteritis, temporal (giant cell arteritis)
- Arthritis
- Ascites
- Asthma
- Ataxia
- Atherosclerosis risk
- Autoimmune brainstem encephalitis
- Autoimmune cerebellar syndrome
- Autoimmune disorders
- Autoimmune dysautonomia
- Autoimmune encephalitis
- Autoimmune hemolytic anemia of the cold type
- Autoimmune hemolytic anemia of the warm type
- Autoimmune hepatitis
- Autoimmune thyreoiditis
- Autoimmune-adrenalitis
- Azoospermia