Cerebral palsy laboratory findings: Difference between revisions
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==Laboratory Findings== | ==Laboratory Findings== | ||
*There are no diagnostic laboratory findings associated with cerebral palsy | |||
*There are no diagnostic laboratory findings associated with | *Following labs may help to rule out other diseases | ||
**Thyroid function tests- to rule out muscle or movement disorders | |||
* | **Lactate and pyruvate levels- may show mitochondrial abnormalities | ||
* | **Organic and amino acids- serum and urine levels may be deranged in inherited metabolic disorders | ||
* | **Ammonia levels- elevated in liver dysfunction or urea cycle defect | ||
** | **Chromosomal analysis | ||
** | ***Karyotype analysis | ||
** | ***Specific DNA testing | ||
**Elevated CSF protein levels | |||
* | **Diagnostic testing for coagulation disorders, if cerebral infarction is suspected | ||
==References== | ==References== |
Revision as of 15:07, 5 October 2017
Cerebral palsy Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
OR
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
OR
[Test] is usually normal among patients with [disease name].
OR
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
OR
There are no diagnostic laboratory findings associated with [disease name].
Laboratory Findings
- There are no diagnostic laboratory findings associated with cerebral palsy
- Following labs may help to rule out other diseases
- Thyroid function tests- to rule out muscle or movement disorders
- Lactate and pyruvate levels- may show mitochondrial abnormalities
- Organic and amino acids- serum and urine levels may be deranged in inherited metabolic disorders
- Ammonia levels- elevated in liver dysfunction or urea cycle defect
- Chromosomal analysis
- Karyotype analysis
- Specific DNA testing
- Elevated CSF protein levels
- Diagnostic testing for coagulation disorders, if cerebral infarction is suspected