Spinocerebellar ataxia- autosomal recessive- with axonal neuropathy

Overview

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy: A rare neurological disorder caused by a genetic defect (chromosome 114q31-q32, recessive) and resulting in ataxia and dysarthria.

Symptoms

* Gait ataxia * Ataxia * Dysarthria * Mild weakness in ends of limbs * Absent tendon reflexes

Diagnosis

Home medical testing related to Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy: * High Cholesterol: Home Testing: o Home Cholesterol Tests o Home Triglycerides Tests o Home Blood Pressure Tests * High Blood Pressure: Home Testing o Home Blood Pressure Monitors o Home Heart Tests * Heart Health: Home Testing: o Heart Rate Monitors o Irregular Heartbeat Detection o Heart Electrocardiogram (ECG) * Thyroid: Home Testing: o Home Thyroid Function Tests o Home TSH Tests o Home Adrenal Function Tests * Diet & Weight Loss: Home Testing: o Home Weight Testing o Home Body Fat Testing (BMI) o Home Body Fat Monitoring o Home Fitness Testing * Diabetes: Related Home Testing: o Home Diabetes Tests o Home Blood Glucose Tests o Home Urine Glucose Tests o Home Urine Ketone Tests o Home Diabetes HbA1c Tests o Home Microalbumin Tests (Kidney) o Home Urine Protein Tests (Kidney) o Home Kidney Tests o Home Eye Tests