Comprehensive Metabolic Panel (CMP) for Mowat-Wilson syndrome due to monosomy 2q22
The comprehensive metabolic panel (cmp) is among the laboratory tests healthcare providers may use to investigate Mowat-Wilson syndrome due to monosomy 2q22. 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 Mowat-Wilson syndrome due to monosomy 2q22
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels.
When evaluating Mowat-Wilson syndrome due to monosomy 2q22, 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 Mowat-Wilson syndrome due to monosomy 2q22
Atypical absence seizure
An atypical absence seizure is a type of generalized non-motor (absence) seizure characterized by interruption...
Constipation
Infrequent or difficult evacuation of feces....
Deeply set eye
An eye that is more deeply recessed into the plane of the face than is typical....
Dysphagia
Difficulty in swallowing....
Episodic vomiting
Paroxysmal, recurrent episodes of vomiting....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Focal-onset seizure
A focal-onset seizure is a type of seizure originating within networks limited to one hemisphere. They may be ...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Urinary incontinence
Loss of the ability to control the urinary bladder leading to involuntary urination....
Other tests used to investigate Mowat-Wilson syndrome due to monosomy 2q22
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 Mowat-Wilson syndrome due to monosomy 2q22?
Yes - the comprehensive metabolic panel (cmp) is among the tests healthcare providers may consider when evaluating Mowat-Wilson syndrome due to monosomy 2q22. 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.