BamforthâLazarus syndrome is a genetic condition that results in
thyroid dysgenesis.[1][2] It is due to
recessive mutations in forkhead/winged-helix domain transcription factor (FKLH15 or TTF2).[3] It is associated with FOXE1.[4]
BamforthâLazarus syndrome is a genetic condition that results in
thyroid dysgenesis.[1][2] It is due to
recessive mutations in forkhead/winged-helix domain transcription factor (FKLH15 or TTF2).[3] It is associated with FOXE1.[4]