Laminin subunit alpha 2-related congenital muscular dystrophy
Laminin subunit alpha 2-related congenital muscular dystrophy is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Laminin subunit alpha 2-related congenital muscular dystrophy
The following symptoms have been associated with Laminin subunit alpha 2-related congenital muscular dystrophy in medical literature. Not everyone experiences the same symptoms.
Cerebral edema
Abnormal accumulation of fluid in the brain....
Dysphagia
Difficulty in swallowing....
Facial palsy
Facial nerve palsy is a dysfunction of cranial nerve VII (the facial nerve) that results in inability to contr...
Focal-onset seizure
A focal-onset seizure is a type of seizure originating within networks limited to one hemisphere. They may be ...
Gastroesophageal reflux
A condition in which the stomach contents leak backwards from the stomach into the esophagus through the lower...
Generalized non-motor (absence) seizure
A generalized non-motor (absence) seizure is a type of a type of dialeptic seizure that is of electrographical...
Hypoventilation
A reduction in the amount of air transported into the pulmonary alveoli by breathing, leading to hypercapnia (...
Intercostal muscle weakness
Lack of strength of the intercostal muscles, i.e., of the muscle groups running along the ribs that create and...
Muscle weakness
Reduced strength of muscles....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tests used to investigate Laminin subunit alpha 2-related congenital muscular dystrophy
Healthcare providers may order these tests when evaluating Laminin subunit alpha 2-related congenital muscular dystrophy. 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 Laminin subunit alpha 2-related congenital muscular dystrophy, which is why a clinical evaluation is important.
Kohlschutter-Tonz syndrome-like
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Morimoto-Ryu-Malicdan neuromuscular syndrome
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intellectual disability, autosomal dominant 43
Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation i...
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...
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...
neurodevelopmental disorder with hypotonia and speech delay, with or without seizures
neurodevelopmental disorder with hypotonia and speech delay, with or without seizures is a medical condition t...
Frequently Asked Questions
What is Laminin subunit alpha 2-related congenital muscular dystrophy?
Laminin subunit alpha 2-related congenital muscular dystrophy is a health condition described in medical literature. Laminin subunit alpha 2-related congenital muscular dystrophy is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Laminin subunit alpha 2-related congenital muscular dystrophy?
Laminin subunit alpha 2-related congenital muscular dystrophy is associated with 10 symptoms in the medical literature we index, including Cerebral edema, Dysphagia, Facial palsy, Focal-onset seizure, Gastroesophageal reflux, Generalized non-motor (absence) seizure. Symptoms vary widely between individuals.
How is Laminin subunit alpha 2-related congenital muscular dystrophy diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Laminin subunit alpha 2-related congenital muscular dystrophy 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 Laminin subunit alpha 2-related congenital muscular dystrophy, please discuss your symptoms with a qualified healthcare provider.