blepharophimosis - intellectual disability syndrome, Verloes type

Blepharophimosis - intellectual disability syndrome, Verloes type is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

The inheritance pattern of this syndrome is autosomal recessive. It is classified as very rare, and there are currently no orphan drugs under investigation for this condition.

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of the autosomal recessive inheritance. Connecting with rare disease registries and online patient communities may provide additional support and resources.