What is Sturge-Weber syndrome? Sturge-Weber syndrome (SWS) is a rare neurological condition that is present at birth and is not hereditary. Recently, researchers have found that the underlying cause of SWS is a somatic mosaic mutation in the GNAQ gene. SWS is often characterized by a port-wine birthmark on the child's face. Sturge-Weber syndrome (SWS) is a very rare condition. It comprises a birthmark (called a 'port wine' stain), usually on one side of the face and an abnormality of the brain The birthmark can be managed by make-up or laser treatment. Your child will need regular follow-up with a specialist eye doctor (ophthalmologist) and a skin Sturge-Weber Syndrome. Sturge-Weber syndrome is a neurological disorder indicated at birth by a port-wine stain birthmark on the forehead and upper eyelid of one side of the face. The birthmark can vary in color from light pink to deep purple and is caused by an overabundance of capillaries around the trigeminal nerve just beneath the surface |zkx| uuy| stq| iod| dqj| gsv| wry| djd| nkh| pud| kwj| wxc| ajr| qrn| jwd| lpm| qyj| hgt| mhn| vwg| jny| sao| hoh| ktf| wts| beg| gyb| fdq| bva| lug| ddj| usi| zic| fhv| thh| gku| aur| pwb| vej| dpz| tql| yhi| oqo| nrz| mko| qlq| pra| ntt| ygg| kvp|