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FOXL2 - blepharophimosis, epicanthus inversus, and ptosis

This test is available for the following conditions:

Conditions > Multiple congenital anomalies (MCA) > Blepharophimosis, epicantus inversus and ptosis

This product is also part of the following panels:

Disorders/differences of sex development (DSD) / Primary adrenal insufficiency panel
Mendelian inherited disorders panel with genome wide CNV analysis
Premature ovarian insufficiency panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method