Moyamoya syndrome with protein S deficiency.

Authors
Category Primary study
JournalEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Year 2000
Moyamoya disease is a cerebrovascular disease with progressive occlusion of both internal carotid arteries and of their branches and formation of a new vascular network at the base of the brain. Because of the angiographic appearance, it is named as moyamoya. The clinical features are cerebral ischaemia, recurrent transient ischaemic attacks, sensorimotor paralysis, convulsions and migraine-like headaches. A 10-year-old child who acutely developed hemiparesis, weakness and aphasia was found to have moyamoya disease and heterozygous protein S deficiency. This case shows us that during the thromboembolic events the coexistence of protein S deficiency and moyamoya should be investigated.
Epistemonikos ID: eaa3b54c7fda0020dcbc3cc7e05c96bdec3f9de3
First added on: Jan 29, 2022