Urinalysis for Autosomal recessive cerebellar ataxia due to STUB1 deficiency
The urinalysis is among the laboratory tests healthcare providers may use to investigate Autosomal recessive cerebellar ataxia due to STUB1 deficiency. Learn what it measures, how to prepare, and what results can tell a provider. Educational content only - not a diagnosis.
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- Sample type
- Urine
- Typical turnaround
- 1-2 business days
- Preparation
- First morning sample preferred; avoid contamination.
Why the urinalysis may be ordered for Autosomal recessive cerebellar ataxia due to STUB1 deficiency
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes.
When evaluating Autosomal recessive cerebellar ataxia due to STUB1 deficiency, a healthcare provider may order the urinalysis alongside other tests based on your symptoms, history, and physical exam. Test selection and result interpretation are clinical decisions made by a qualified professional.
Symptoms associated with Autosomal recessive cerebellar ataxia due to STUB1 deficiency
Alopecia
A noncongenital process of hair loss, which may progress to partial or complete baldness....
Dysphagia
Difficulty in swallowing....
Hand tremor
An unintentional, oscillating to-and-fro muscle movement affecting the hand....
Head tremor
An unintentional, oscillating to-and-fro muscle movement affecting head movement....
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Memory impairment
An impairment of memory as manifested by a reduced ability to remember things such as dates and names, and inc...
Postural tremor
A type of tremors that is triggered by holding a limb in a fixed position....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Other tests used to investigate Autosomal recessive cerebellar ataxia due to STUB1 deficiency
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Frequently Asked Questions
Is the urinalysis used to investigate Autosomal recessive cerebellar ataxia due to STUB1 deficiency?
Yes - the urinalysis is among the tests healthcare providers may consider when evaluating Autosomal recessive cerebellar ataxia due to STUB1 deficiency. Examines urine content to help detect urinary tract infections, kidney disease, and diabetes. Test selection is a clinical decision made by a qualified professional.
How should I prepare for the urinalysis?
First morning sample preferred; avoid contamination.
How long does the urinalysis take?
Results for the urinalysis are typically available within 1-2 business days depending on the laboratory.
Does this website interpret my urinalysis result?
No. SymptomDatabase.com does not interpret laboratory results. Discuss all results with a qualified healthcare provider.