hereditary spastic paraplegia 12

Autosomal dominant spastic paraplegia type 12 is a pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.

Also known as: RTN2 hereditary spastic paraplegia, SPG12, autosomal dominant spastic paraplegia type 12, hereditary spastic paraplegia caused by mutation in RTN2, hereditary spastic paraplegia type 12, spastic paraplegia 12, spastic paraplegia 12, autosomal dominant.

Category: General

Looking into hereditary spastic paraplegia 12? See the lab tests healthcare providers may use to investigate hereditary spastic paraplegia 12, and learn what each one measures.
Explore tests for hereditary spastic paraplegia 12
Symptoms

Symptoms associated with hereditary spastic paraplegia 12

The following symptoms have been associated with hereditary spastic paraplegia 12 in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate hereditary spastic paraplegia 12

Healthcare providers may order these tests when evaluating hereditary spastic paraplegia 12. 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...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with hereditary spastic paraplegia 12, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is hereditary spastic paraplegia 12?

hereditary spastic paraplegia 12 is a health condition described in medical literature. Autosomal dominant spastic paraplegia type 12 is a pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.

What are the symptoms of hereditary spastic paraplegia 12?

hereditary spastic paraplegia 12 is associated with 7 symptoms in the medical literature we index, including Chronic constipation, Diplopia, Dysphagia, Lower limb muscle weakness, Myalgia, Seizure. Symptoms vary widely between individuals.

How is hereditary spastic paraplegia 12 diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with hereditary spastic paraplegia 12 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 hereditary spastic paraplegia 12, please discuss your symptoms with a qualified healthcare provider.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.