Stormorken syndrome

Stormorken-Sjaastad-Langslet syndrome is characterized by thrombocytopathy, asplenia, miosis, muscle fatigue, migraine, dyslexia, and ichthyosis. It has been described in six members of one family. It is transmitted as an autosomal dominant trait.

Also known as: Stormorken syndrome, Thrombocytopathy-asplenia-miosis syndrome, STRMK, Stormorken-Sjaastad-Langslet syndrome, Thrombocytopathy asplenia miosis, Thrombocytopathy, asplenia, and miosis, york Platelet syndrome

2 clinical trials for this condition and its sub-types.