Autosomal recessive cerebellar ataxia due to STUB1 deficiency
Autosomal recessive cerebellar ataxia due to STUB1 deficiency is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Autosomal recessive cerebellar ataxia due to STUB1 deficiency
The following symptoms have been associated with Autosomal recessive cerebellar ataxia due to STUB1 deficiency in medical literature. Not everyone experiences the same symptoms.
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 ...
Tests used to investigate Autosomal recessive cerebellar ataxia due to STUB1 deficiency
Healthcare providers may order these tests when evaluating Autosomal recessive cerebellar ataxia due to STUB1 deficiency. Test selection is a clinical decision made by a qualified professional.
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 ...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Conditions with overlapping symptoms
These conditions share symptoms with Autosomal recessive cerebellar ataxia due to STUB1 deficiency, which is why a clinical evaluation is important.
Jaberi-Elahi syndrome
Jaberi-Elahi syndrome is a medical condition that may be associated with various symptoms and signs....
Stolerman neurodevelopmental syndrome
Stolerman neurodevelopmental syndrome is a medical condition that may be associated with various symptoms and ...
Tay-Sachs disease
Tay-Sachs disease is a medical condition that may be associated with various symptoms and signs....
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...
spinocerebellar ataxia 52
spinocerebellar ataxia 52 is a medical condition that may be associated with various symptoms and signs....
spinocerebellar ataxia type 29
Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA ...
Frequently Asked Questions
What is Autosomal recessive cerebellar ataxia due to STUB1 deficiency?
Autosomal recessive cerebellar ataxia due to STUB1 deficiency is a health condition described in medical literature. Autosomal recessive cerebellar ataxia due to STUB1 deficiency is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Autosomal recessive cerebellar ataxia due to STUB1 deficiency?
Autosomal recessive cerebellar ataxia due to STUB1 deficiency is associated with 8 symptoms in the medical literature we index, including Alopecia, Dysphagia, Hand tremor, Head tremor, Hearing impairment, Memory impairment. Symptoms vary widely between individuals.
How is Autosomal recessive cerebellar ataxia due to STUB1 deficiency diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Autosomal recessive cerebellar ataxia due to STUB1 deficiency include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have Autosomal recessive cerebellar ataxia due to STUB1 deficiency, please discuss your symptoms with a qualified healthcare provider.