autosomal recessive hyperinsulinism due to SUR1 deficiency

autosomal recessive hyperinsulinism due to SUR1 deficiency is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

The condition is also referred to as autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency. Currently, there are no orphan drug designations under investigation for this condition.

Patients and caregivers are encouraged to seek genetic counseling due to the inherited nature of this condition. Connecting with rare disease registries such as Orphanet may provide additional resources and support. Finding specialists experienced with hyperinsulinism can also be beneficial.