Diagnostic Challenge of Sturge Weber Syndrome Phenotype in Camp Setting
Sturge Weber angiomatosis is a non-developmental, rare condition with a vascular hamartomata's involving the tissues of brain and face. We report herewith a case presenting with recurrent seizures and facial port wine stain in a camp of tribal area in Central India. This patient presentation mi...
Saved in:
| Main Authors: | Annvi singh, Rahul Kumar Gupta, Ashwani Tandon |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2022-01-01
|
| Series: | NMO Journal |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.53772/NMO.2022.16113 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Sturge Weber Syndrome – Roach’s Type II Variant
by: Muna Bista, et al.
Published: (2020-10-01) -
Sturge Weber Syndrome – Roach’s Type II Variant
by: Muna Bista, et al.
Published: (2020-10-01) -
Atypical imaging features of sturge-weber syndrome in a 10-month-old infant: A case report
by: Biruk T. Mengistie, et al.
Published: (2025-06-01) -
Bilateral Ocular and Facial with Unilateral Intracranial Involvement In Sturge Weber Syndrome: A Case Report and Review of Literature
by: Mihika Dube, et al.
Published: (2017-04-01) -
Surgical treatment of drug resistant epilepsy in Sturge-Weber syndrome: review of the literature and clinical case presentation
by: G. S. Ibatova, et al.
Published: (2019-04-01)