A 17-month-old boy from San Antonio, Texas, has been diagnosed with Farber disease, an ultra-rare genetic disorder, and his family has launched a fundraising campaign to support his medical care.
The child, identified as Zayd, received the diagnosis after medical evaluations and genetic testing confirmed mutations associated with Farber disease. The disorder is a lysosomal storage condition that affects the breakdown of fats in the body and can impact joints, tissues, and the nervous system.
Zayd’s family is raising funds to cover medical expenses, therapies, specialized equipment, and other related costs. The campaign is shared through community networks and online platforms.
Medical specialists continue to monitor Zayd’s condition and adjust care as needed. Farber disease is inherited in an autosomal recessive pattern, and genetic counselors have advised the family on recurrence risks.
