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Sturge-Weber Syndrome: A Rare Case Report
Darshankumar M Raval1, Vaishnavi M Rathod1, Anjali B Patel1
1Department of General Medicine, Sir Sayaji General (SSG) Hospital, Medical College Baroda, Vadodara, IND.
Sturge-Weber syndrome (SWS) is a rare neurocutaneous disorder causing facial angiomas and brain abnormalities. Early diagnosis via imaging and history is crucial for managing symptoms like seizures.
Area of Science:
- Neuroscience
- Genetics
- Dermatology
Background:
- Sturge-Weber syndrome (SWS) is a rare, sporadic neurocutaneous disorder.
- It is characterized by facial angiomas (port-wine stains), particularly in the trigeminal nerve distribution, and intracranial leptomeningeal angiomas.
- Seizures are the most common presenting symptom, with onset varying from birth to adulthood.
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