Muscular dystrophy, limb-girdle, type 1E
Muscular dystrophy, limb-girdle, type 1E is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Muscular dystrophy, limb-girdle, type 1E
The following symptoms have been associated with Muscular dystrophy, limb-girdle, type 1E in medical literature. Not everyone experiences the same symptoms.
Bulbar palsy
Bulbar weakness (or bulbar palsy) refers to bilateral impairment of function of the lower cranial nerves IX, X...
Dysphagia
Difficulty in swallowing....
Dyspnea
Difficult or labored breathing. Dyspnea is a subjective feeling only the patient can rate, e.g., on a Borg sca...
Facial palsy
Facial nerve palsy is a dysfunction of cranial nerve VII (the facial nerve) that results in inability to contr...
Myalgia
Pain in muscle....
Pelvic girdle muscle weakness
Weakness of the muscles of the pelvic girdle (also known as the hip girdle), that is, lack of strength of the ...
Shoulder girdle muscle weakness
The shoulder, or pectoral, girdle is composed of the clavicles and the scapulae. Shoulder-girdle weakness refe...
Tests used to investigate Muscular dystrophy, limb-girdle, type 1E
Healthcare providers may order these tests when evaluating Muscular dystrophy, limb-girdle, type 1E. 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 Muscular dystrophy, limb-girdle, type 1E, which is why a clinical evaluation is important.
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive external ophthalmoplegia is a medical condition that may be associated with var...
Brown-Vialetto-van Laere syndrome 1
Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene....
Idiopathic hypereosinophilic syndrome
Idiopathic hypereosinophilic syndrome is a medical condition that may be associated with various symptoms and ...
Steinert myotonic dystrophy
Steinert myotonic dystrophy is a medical condition that may be associated with various symptoms and signs....
mitochondrial DNA deletion syndrome with progressive myopathy
mitochondrial DNA deletion syndrome with progressive myopathy is a medical condition that may be associated wi...
muscular dystrophy-dystroglycanopathy type B5
A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with va...
Frequently Asked Questions
What is Muscular dystrophy, limb-girdle, type 1E?
Muscular dystrophy, limb-girdle, type 1E is a health condition described in medical literature. Muscular dystrophy, limb-girdle, type 1E is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Muscular dystrophy, limb-girdle, type 1E?
Muscular dystrophy, limb-girdle, type 1E is associated with 7 symptoms in the medical literature we index, including Bulbar palsy, Dysphagia, Dyspnea, Facial palsy, Myalgia, Pelvic girdle muscle weakness. Symptoms vary widely between individuals.
How is Muscular dystrophy, limb-girdle, type 1E diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Muscular dystrophy, limb-girdle, type 1E 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 Muscular dystrophy, limb-girdle, type 1E, please discuss your symptoms with a qualified healthcare provider.