Comprehensive Metabolic Panel (CMP) for PMM2-congenital disorder of glycosylation
The comprehensive metabolic panel (cmp) is among the laboratory tests healthcare providers may use to investigate PMM2-congenital disorder of glycosylation. 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 PMM2-congenital disorder of glycosylation
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels.
When evaluating PMM2-congenital disorder of glycosylation, 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 PMM2-congenital disorder of glycosylation
Diarrhea
Abnormally increased frequency (usually defined as three or more) loose or watery bowel movements a day....
Edema
An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Generalized-onset seizure
A generalized-onset seizure is a type of seizure originating at some point within, and rapidly engaging, bilat...
Intention tremor
A type of kinetic tremor that occurs during target directed movement is called intention tremor. That is, an o...
Muscle weakness
Reduced strength of muscles....
Pericarditis
Inflammation of the sac-like covering around the heart (pericardium)....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tremor
An unintentional, oscillating to-and-fro muscle movement about a joint axis....
Vomiting
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic...
Other tests used to investigate PMM2-congenital disorder of glycosylation
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 PMM2-congenital disorder of glycosylation?
Yes - the comprehensive metabolic panel (cmp) is among the tests healthcare providers may consider when evaluating PMM2-congenital disorder of glycosylation. 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.