eMedicine Specialties > Physical Medicine and Rehabilitation > Medical Diseases
Cerebral Palsy: Differential Diagnoses & Workup
Updated: Mar 11, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Differential Diagnoses
Other Problems to Be Considered
Metabolic and genetic diseases
Workup
Laboratory Studies
- There are no definitive lab studies for diagnosing cerebral palsy, only studies to rule out other symptom causes, such as metabolic or genetic abnormalities, as deemed necessary based on clinical examination.
- Thyroid studies
- Lactate level
- Pyruvate level
- Organic and amino acids
- Chromosomes
- Cerebrospinal protein - Levels may assist in determining asphyxia in the neonatal period. Protein levels can be elevated, as can the lactate-to-pyruvate ratio.
Imaging Studies
- Neuroimaging studies can help to evaluate brain damage and to identify persons who are at risk for cerebral palsy. Data to support a definitive diagnosis of cerebral palsy are lacking.
- Neonatal ultrasonography provides information about the ventricular system, basal ganglia, and corpus callosum, as well as diagnostic information on intraventricular hemorrhage and hypoxic-ischemic injury to the periventricular white matter. Periventricular leukomalacia initially appears as an echodense area that converts to an echolucent area when the patient is approximately age 2 weeks. Periventricular leukomalacia is strongly associated with cerebral palsy. (See image below and Image 2.)
- Computed tomography (CT) scanning provides information to help in diagnosing congenital malformations, intracranial hemorrhages, and periventricular leukomalacia, especially in the infant.
- Magnetic resonance imaging (MRI) is most useful after 2-3 weeks of life. MRI is the best study for assessing white matter disease in an older child.
- Evoked potentials are used to evaluate the anatomic pathways of the auditory and visual systems.
- A normal brain imaging study does not mean that the child does not have cerebral palsy, since the diagnosis is always based only on physical exam findings.
Magnetic resonance imaging (MRI) scan of a 1-year-old boy who was born at gestational week 27. Clinical examination is consistent with spastic diplegic cerebral palsy. Pseudocolpocephaly and decreased volume of the white matter posteriorly are consistent with periventricular leukomalacia. Evidence of diffuse polymicrogyria and thinning of the corpus callosum is noted.
Related eMedicine topics:
Periventricular Leukomalacia [Pediatrics: Cardiac Disease and Critical Care Medicine]
Periventricular Leukomalacia [Radiology]
Other Tests
- Hearing and vision screens may be helpful.
- Electroencephalography is useful in evaluating severe hypoxic-ischemic injury. Findings initially show marked suppression of amplitude and slowing, followed by a discontinuous pattern of voltage suppression, with bursts of high-voltage sharp and slow waves at 24-48 hours.
More on Cerebral Palsy |
| Overview: Cerebral Palsy |
Differential Diagnoses & Workup: Cerebral Palsy |
| Treatment & Medication: Cerebral Palsy |
| Follow-up: Cerebral Palsy |
| Multimedia: Cerebral Palsy |
| References |
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References
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Further Reading
Keywords
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Differential Diagnoses & Workup: Cerebral Palsy