ABSTRACT Sturge-Weber syndrome is a rare sporadic and congenital neurocutaneous disease characterized primarily by the presence of cutaneous and extracutaneous capillary malformations. Our understanding of this syndrome has improved since its first description over the years, particularly with the identification of different clinical presentations and new genetic mutations. Ocular manifestations are frequently observed in this syndrome but often develop insidiously and can threaten visual prognosis. Thus, an appreciation of different ophthalmological manifestations seems crucial. In the same perspective, we report […]

Sturge-Weber Syndrome is a rare neuro-oculocutaneous disorder. The authors describe the case of a 13 years old boy, presented with bilateral Sturge-Weber Syndrome and glaucoma. Surgical treatment with Ahmed valve implantation in both eyes was carried out achieving lower levels of intraocular pressure.

A síndrome de Sturge-Weber trata-se de uma doença neuro-óculocutânea rara. Os autores relatam o caso de um paciente do sexo masculino, de 13 anos de idade, que se apresentou com Síndrome de Sturge-Weber bilateral e glaucoma. Foi realizado o tratamento cirúrgico com implante de válvula de Ahmed em ambos os olhos e alcançado a redução da pressão intraocular bilateral.