Sturge- Weber Syndrome in a 28-Year-Old Tanzanian Female: A Case Report

Authors

  • Sarah Shali Matuja

  • Maryam Amour

  • Evangelista Malindisa

  • William Matuja

Keywords:

sturge weber syndrome, seizures, port-wine stain, angiomas

Abstract

Background: Sturge Weber Syndrome is a sporadic neurocutaneous disorder of elusive etiology which is characterized by a vast continuum of manifestations ranging from neurological, cutaneous and ocular features. The main complications of the disorder include epileptic seizures, hemi paresis, and delayed neuropsychological development leading to poor quality of life. Case presentation: We present a 28 years old female of African descent who was seen at

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How to Cite

Sturge- Weber Syndrome in a 28-Year-Old Tanzanian Female: A Case Report. (2020). Global Journal of Medical Research, 20(F9), 1-5. https://medicalresearchjournal.org/index.php/GJMR/article/view/2232

 

References

Sturge- Weber Syndrome in a 28-Year-Old Tanzanian Female: A Case Report

Published

2020-08-15

Issue

Vol. 20 No. F9 (2020): GJMR-F Diseases: Volume 20 Issue F9

Section

Articles

License

Copyright (c) 2020 Authors and Global Journals Private Limited

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

Sturge- Weber Syndrome in a 28-Year-Old Tanzanian Female: A Case Report. (2020). Global Journal of Medical Research, 20(F9), 1-5. https://medicalresearchjournal.org/index.php/GJMR/article/view/2232