In addition to
Sturge-Weber syndrome, this category includes such rare entities as Klippel-Trenaunay syndrome (CM + VM +/- LM + limb overgrowth), Proteus syndrome (CM, VM and/or LM + asymmetric somatic overgrowth) and Maffucci syndrome (VM +/- spindle cell hemangioma + enchondroma).
Brain CT which was performed with the pre-diagnosis of
Sturge-Weber syndrome revealed calcifications in the involved hemisphere (Figure 2b).
Pathophysiology of
Sturge-Weber syndrome. J Child Neurol 2003;18:509-516.
Pathophysiology, diagnosis, and management of glaucoma associated with
Sturge-Weber syndrome. Int Ophthalmol 2017;[Epub ahead of print].
Sturge-Weber syndrome (SWS), or encephalotrigeminal angiomatosis, is a rare, congenital neurocutaneous syndrome characterized by unilateral facial cutaneous vascular malformation (nevus flammeus or port-wine stain [PWS]) in association with ipsilateral leptomeningeal angiomatosis.
Sturge-Weber syndrome is a sporadic, congenital neurocutaneous syndrome, characterised by the association of ipsilateral facial angioma in the distribution of the trigeminal nerve with angiomatosis of the leptomeninges.
Annie, from Barkisland, has a rare neurological condition called
Sturge-Weber Syndrome which causes her to suffer several epileptic seizures every day.
Yasmin suffers from
Sturge-Weber syndrome, a rare condition affecting the skin, brain and eyes.
The eight-year-old suffers from rare
Sturge-Weber syndrome, which affects the skin, eyes and brain.
Differential diagnosis to be considered in a patient with cerebral hemiatrophy include
Sturge-Weber syndrome, Rasmussen encephalitis, Silver-Russel syndrome, and basal ganglia germinoma.
Heterochromia iridis and pertinent clinical findings in patients with glaucoma associated with
sturge-weber syndrome. J Pediatr Ophthalmol Strabismus.