atrial fibrillation, familial, 2

atrial fibrillation, familial, 2 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

This condition is also known as ATFB2 and is classified under the OMIM entry 608988. It is inherited in an autosomal dominant manner. There are currently no orphan drug designations under investigation for this condition.

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of the autosomal dominant inheritance. Connecting with rare disease registries, such as NORD or Orphanet, may provide additional resources and support. Finding specialists experienced with atrial fibrillation or similar conditions can also be beneficial.