Alpha-N-acetylgalactosaminidase deficiency type 1
Alpha-N-acetylgalactosaminidase deficiency type 1 is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Alpha-N-acetylgalactosaminidase deficiency type 1
The following symptoms have been associated with Alpha-N-acetylgalactosaminidase deficiency type 1 in medical literature. Not everyone experiences the same symptoms.
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Hemiplegia/hemiparesis
Loss of strength in the arm, leg, and sometimes face on one side of the body. Hemiplegia refers to a severe or...
Lymphedema
Localized fluid retention and tissue swelling caused by a compromised lymphatic system....
Muscle weakness
Reduced strength of muscles....
Paresthesia
Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Vertigo
An abnormal sensation of spinning while the body is actually stationary....
Tests used to investigate Alpha-N-acetylgalactosaminidase deficiency type 1
Healthcare providers may order these tests when evaluating Alpha-N-acetylgalactosaminidase deficiency type 1. 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 Alpha-N-acetylgalactosaminidase deficiency type 1, which is why a clinical evaluation is important.
Fabry disease
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Familial or sporadic hemiplegic migraine
Familial or sporadic hemiplegic migraine is a medical condition that may be associated with various symptoms a...
Gitelman syndrome
Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalem...
Krabbe disease
Krabbe disease is a medical condition that may be associated with various symptoms and signs....
Morimoto-Ryu-Malicdan neuromuscular syndrome
Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...
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 Alpha-N-acetylgalactosaminidase deficiency type 1?
Alpha-N-acetylgalactosaminidase deficiency type 1 is a health condition described in medical literature. Alpha-N-acetylgalactosaminidase deficiency type 1 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Alpha-N-acetylgalactosaminidase deficiency type 1?
Alpha-N-acetylgalactosaminidase deficiency type 1 is associated with 7 symptoms in the medical literature we index, including Hearing impairment, Hemiplegia/hemiparesis, Lymphedema, Muscle weakness, Paresthesia, Seizure. Symptoms vary widely between individuals.
How is Alpha-N-acetylgalactosaminidase deficiency type 1 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Alpha-N-acetylgalactosaminidase deficiency type 1 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 Alpha-N-acetylgalactosaminidase deficiency type 1, please discuss your symptoms with a qualified healthcare provider.