alopecia areata 2

Alopecia areata 2 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

The condition is known by several synonyms, including AA2. It is associated with multifactorial, autosomal recessive, and autosomal dominant inheritance patterns. There are currently no orphan drugs under investigation for this condition.

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