Comprehensive Metabolic Panel (CMP) for congenital muscular dystrophy due to LMNA mutation
The comprehensive metabolic panel (cmp) is among the laboratory tests healthcare providers may use to investigate congenital muscular dystrophy due to LMNA mutation. Learn what it measures, how to prepare, and what results can tell a provider. Educational content only - not a diagnosis.
Order a Comprehensive Metabolic Panel (CMP) Test
Lab testing is available through our partner network. Order online and visit a local collection site. No doctor's order or insurance required.
- 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 congenital muscular dystrophy due to LMNA mutation
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels.
When evaluating congenital muscular dystrophy due to LMNA mutation, 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 congenital muscular dystrophy due to LMNA mutation
Axial muscle weakness
Reduced strength of the axial musculature (i.e., of the muscles of the head and neck, spine, and ribs)....
Distal muscle weakness
Reduced strength of the musculature of the distal extremities....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Neck muscle weakness
Decreased strength of the neck musculature....
Proximal muscle weakness
A lack of strength of the proximal muscles....
Respiratory insufficiency due to muscle weakness
Information about Respiratory insufficiency due to muscle weakness....
Upper limb muscle weakness
Weakness of the muscles of the arms....
Other tests used to investigate congenital muscular dystrophy due to LMNA mutation
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 congenital muscular dystrophy due to LMNA mutation?
Yes - the comprehensive metabolic panel (cmp) is among the tests healthcare providers may consider when evaluating congenital muscular dystrophy due to LMNA mutation. 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.