Urinalysis for PMM2-congenital disorder of glycosylation
The urinalysis 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
- Urine
- Typical turnaround
- 1-2 business days
- Preparation
- First morning sample preferred; avoid contamination.
Why the urinalysis may be ordered for PMM2-congenital disorder of glycosylation
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes.
When evaluating PMM2-congenital disorder of glycosylation, a healthcare provider may order the urinalysis 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...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Frequently Asked Questions
Is the urinalysis used to investigate PMM2-congenital disorder of glycosylation?
Yes - the urinalysis is among the tests healthcare providers may consider when evaluating PMM2-congenital disorder of glycosylation. Examines urine content to help detect urinary tract infections, kidney disease, and diabetes. Test selection is a clinical decision made by a qualified professional.
How should I prepare for the urinalysis?
First morning sample preferred; avoid contamination.
How long does the urinalysis take?
Results for the urinalysis are typically available within 1-2 business days depending on the laboratory.
Does this website interpret my urinalysis result?
No. SymptomDatabase.com does not interpret laboratory results. Discuss all results with a qualified healthcare provider.