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Colegio de Medicos y Cirujanos República de Costa Rica

2015, Number 617

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Rev Med Cos Cen 2015; 72 (617)

Síndrome de Sturge Weber

Hernández LM, Herrera SK

Language: Spanish
References: 11
Page: 729-731
PDF size: 151.83 Kb.


ABSTRACT

Sturge Weber (encefalotrigeminal angiomatosis) is a neurocutaneous disorder characterized by a clinical triad of leptomeningeal angioma (cerebral vascular malformation), port wine nevus (facial vascular malformation) and ocular vascular malformation that can lead to glaucoma. Other clinical manifestations such as seizures, hemiparesis, stroke, mental delay, can worsen the prognosis according to their severity.


REFERENCES

  1. Alkonyi Balint, MD, Chugani Harry T., MD, Karia Samir, MD, Behen Michael E., PhD, and Juhasz Csaba MD, PhD. “Clinical Outcomes in Bilateral Sturge-Weber Syndrome”. ELSEVEIR Pediatric Neurolgy. 44. July 2011.

  2. Chen Ling, M.D., Wu Jinjin, M.D., Ph.D., Xu Minhui, M.D., Ph.D.1, Chen Nian, M.D., Yang Yadong, M.D., Ph.D. “Sturge-Weber Syndrome” Departments of Dermatology and Neurosurgery, Daping Hospital, Third Military Medical University, Chongqing, China Ann. Dermatol Vol. 23, No. 4, 2011.

  3. Collettini Federico, Diederichs Gerd, Gebauer Bernhard, Poellinger Alexander “Sturge-Weber Syndrome”. Department of Diagnostic and Interventional Radiology at a Campus Mitte and b Campus Virchow,Charité, Berlin , Germany. Pediatr Neurosurg 2011;47:80 DOI: 10.1159/000329631

  4. Comi Anne M., MD “Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome”. The Neurologist. 17 (4), July 2011. 180-181.

  5. Gill Namrata C., Bhaskar Nandini. “Sturger-Weber síndrome: A case report”. Contemporary Clinical Dentistry. 1(3). Septiembre 2010. 182,184-185

  6. Irving Natasha D., BA, Lim Jae Hyung, BA, Cohen Bernard, MD, Ferenc Lisa M., MA, and Comi Anne M., MD. “Sturge-Weber Syndrome: Ear, Nose, and Throat Issues and Neurologic Status” ELSEVIER Pediatr Neurol 2010;43:241-244.

  7. Jagtap Sujit, Srinivas G., Harsha K. J., Radhakrishnan Neelima and Radhakrishnan Ashalatha “Sturge-Weber Syndrome: Clinical Spectrum, Disease Course, and Outcome of 30 Patients”. Journal of Child Neurology. 1(7). Mayo 2012. 2,3- 5

  8. Lo Warren, Marchuk Douglas, Ball Karen L, Juh Csaba, Jordan Lori , Ewen Joshua, Comi. Anne “Updates and future horizons on the understanding, diagnosis, and treatment of Sturge–Weber syndrome brain involvement” . Developmental Medicine & Child Neurology. 54(21). 216,217-22

  9. Montes Ana Milena, Toro Ana Milena, Arredondo María Isabel, Arroyave Juan Esteban, Vásquez Luz Adriana, Molina Verónica. “Síndrome de Sturge-Weber tratado con láser de colorante pulsado” Rev Asoc Colomb Dermatol Rev Asoc Colomb Dermatol. 2010;18: 236-8.

  10. Rios M., Barbot C., P.S. Pinto, Salício L. , Santos M., Carrilho I. y Temudo T. “Síndrome de Sturge-Weber: variabilidad clínica y de neuroimagen”.Analisis de pediatría. 77, marzo 2012. 398,400-401.

  11. Vila M.T.. Servicio de Neuropediatría, Hospital Universitaria Politecnic La Fe, Valencia, España. “Stroke like» episodes in Sturge-Weber syndrome” ELSEVIER An Pediatr (Barc). 2013 ANPEDI-1298.




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