Stormorken syndrome

MONDO:0008497

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, 0 tagged with Stormorken syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic constitutional thrombocytopenia (8)

Including sub-types (2) Tagged with Stormorken syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.