GM1 gangliosidosis
GM1 gangliosidosis is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with GM1 gangliosidosis
The following symptoms have been associated with GM1 gangliosidosis in medical literature. Not everyone experiences the same symptoms.
Arthralgia
Joint pain....
Blindness
Blindness is the condition of lacking visual perception defined as a profound reduction in visual perception. ...
Dysphagia
Difficulty in swallowing....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Gastroesophageal reflux
A condition in which the stomach contents leak backwards from the stomach into the esophagus through the lower...
Generalised tonic-clonic seizure without focal onset
A bilateral tonic-clonic seizure with generalized onset is a type of bilateral tonic-clonic seizure characteri...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tremor
An unintentional, oscillating to-and-fro muscle movement about a joint axis....
Weight loss
Reduction of total body weight....
Tests used to investigate GM1 gangliosidosis
Healthcare providers may order these tests when evaluating GM1 gangliosidosis. 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 GM1 gangliosidosis, which is why a clinical evaluation is important.
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Jaberi-Elahi syndrome
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Wilson disease
Wilson disease is a medical condition that may be associated with various symptoms and signs....
intellectual disability, autosomal dominant 43
Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation i...
multiple mitochondrial dysfunctions syndrome 9b
A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is c...
Frequently Asked Questions
What is GM1 gangliosidosis?
GM1 gangliosidosis is a health condition described in medical literature. GM1 gangliosidosis is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of GM1 gangliosidosis?
GM1 gangliosidosis is associated with 9 symptoms in the medical literature we index, including Arthralgia, Blindness, Dysphagia, Failure to thrive, Gastroesophageal reflux, Generalised tonic-clonic seizure without focal onset. Symptoms vary widely between individuals.
How is GM1 gangliosidosis diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with GM1 gangliosidosis 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 GM1 gangliosidosis, please discuss your symptoms with a qualified healthcare provider.