Comprehensive Metabolic Panel (CMP) for autosomal recessive limb-girdle muscular dystrophy type 2H
The comprehensive metabolic panel (cmp) is among the laboratory tests healthcare providers may use to investigate autosomal recessive limb-girdle muscular dystrophy type 2H. Learn what it measures, how to prepare, and what results can tell a provider. Educational content only - not a diagnosis.
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- Sample type
- Blood
- Typical turnaround
- 1-2 business days
- Preparation
- Fasting may be required for 8-12 hours.
Why the comprehensive metabolic panel (cmp) may be ordered for autosomal recessive limb-girdle muscular dystrophy type 2H
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels.
When evaluating autosomal recessive limb-girdle muscular dystrophy type 2H, a healthcare provider may order the comprehensive metabolic panel (cmp) alongside other tests based on your symptoms, history, and physical exam. Test selection and result interpretation are clinical decisions made by a qualified professional.
Symptoms associated with autosomal recessive limb-girdle muscular dystrophy type 2H
Exercise-induced myalgia
The occurrence of an unusually high amount of muscle pain following exercise....
Facial palsy
Facial nerve palsy is a dysfunction of cranial nerve VII (the facial nerve) that results in inability to contr...
Neck flexor weakness
Weakness of the muscles involved in neck flexion (sternocleidomastoid, longus capitus, longus colli, and scale...
Paresthesia
Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause....
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 ...
Proximal muscle weakness
A lack of strength of the proximal muscles....
Quadriceps muscle weakness
Weakness of the quadriceps muscle (that is, of the muscle fasciculus of quadriceps femoris)....
Shoulder girdle muscle weakness
The shoulder, or pectoral, girdle is composed of the clavicles and the scapulae. Shoulder-girdle weakness refe...
Other tests used to investigate autosomal recessive limb-girdle muscular dystrophy type 2H
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Frequently Asked Questions
Is the comprehensive metabolic panel (cmp) used to investigate autosomal recessive limb-girdle muscular dystrophy type 2H?
Yes - the comprehensive metabolic panel (cmp) is among the tests healthcare providers may consider when evaluating autosomal recessive limb-girdle muscular dystrophy type 2H. Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels. Test selection is a clinical decision made by a qualified professional.
How should I prepare for the comprehensive metabolic panel (cmp)?
Fasting may be required for 8-12 hours.
How long does the comprehensive metabolic panel (cmp) take?
Results for the comprehensive metabolic panel (cmp) are typically available within 1-2 business days depending on the laboratory.
Does this website interpret my comprehensive metabolic panel (cmp) result?
No. SymptomDatabase.com does not interpret laboratory results. Discuss all results with a qualified healthcare provider.