👉 Hemeralopia is a rare genetic condition that occurs in only one out of every 10,000 newborns. It is characterized by a distinctive facial appearance and difficulty with speech and swallowing. Hemeralopia can be caused by mutations in the gene responsible for producing dopamine, which is involved in speech and movement control. This condition can cause significant challenges for individuals with hemeralopia, including difficulties with communication, coordination, and balance. Treatment options for hemeralopia include medication to
