Fechtner syndrome

Fechtner syndrome is a variant of Alport syndrome with leukocyte inclusions and macrothrombocytopenia.[1]

References

  1. ↑ cause by mutation in the MYH9 gene on chromosome 22q11Peterson LC, Rao KV, Crosson JT, White JG (February 1985). "Fechtner syndrome--a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia". Blood 65 (2): 397–406. PMID 2981587. Retrieved 2013-05-19.