alopecia-intellectual disability syndrome 3

Alopecia-intellectual disability syndrome 3 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

The condition is also known as APMR3 and is characterized by autosomal recessive inheritance. Currently, there are no known associated genes or documented symptoms, and no orphan drugs are under investigation.

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