Porencephaly
(Redirected from Familial porencephaly)
Porencephaly | |
---|---|
Synonyms | |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Seizures, developmental delay, motor impairment, spasticity |
Complications | Hydrocephalus, cerebral palsy |
Onset | Congenital or acquired |
Duration | Lifelong |
Types | N/A |
Causes | Stroke, infection, trauma, genetic disorders |
Risks | |
Diagnosis | MRI, CT scan |
Differential diagnosis | Schizencephaly, hydranencephaly, arachnoid cyst |
Prevention | N/A |
Treatment | Anticonvulsants, physical therapy, occupational therapy, speech therapy |
Medication | N/A |
Prognosis | Variable, depends on severity |
Frequency | Rare |
Deaths | N/A |
Porencephaly is a rare neurological disorder characterized by the presence of cysts or cavities within the cerebral hemisphere. These cysts or cavities are usually the result of damage from stroke or infections that occur before birth.
Causes[edit | edit source]
The exact cause of porencephaly is unknown. However, it is believed to be associated with a variety of factors including genetic mutation, intrauterine infection, trauma, and ischemia.
Symptoms[edit | edit source]
Symptoms of porencephaly can vary greatly depending on the size and location of the cyst or cavity. Common symptoms include developmental delay, motor impairment, seizures, hydrocephalus, spasticity, and microcephaly.
Diagnosis[edit | edit source]
Diagnosis of porencephaly is typically made through imaging studies such as MRI or CT scan. These tests can reveal the presence of cysts or cavities in the brain.
Treatment[edit | edit source]
There is no cure for porencephaly. Treatment is symptomatic and supportive, and may include physical therapy, occupational therapy, speech therapy, and medication to control seizures.
Prognosis[edit | edit source]
The prognosis for individuals with porencephaly varies widely. Some individuals may have normal intelligence and lifespan, while others may have severe disabilities and shortened lifespan.
See also[edit | edit source]
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