Fechtner syndrome | |
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Other names | Alport syndrome with leukocyte inclusions and macrothrombocytopenia |
Fechtner syndrome is inherited in an autosomal dominant manner. |
Fechtner syndrome is a variant of Alport syndrome characterized by leukocyte inclusions, macrothrombocytopenia,[1]thrombocytopenia, nephritis, and sensorineural hearing loss.[2] Some patients may also develop cataracts.[3]