Chromosome 10p Terminal Deletion Syndrome


Type of disease: Rare conditions

Chromosome 10p terminal deletion syndrome is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This genetic defect can result in a variety of birth defects. Birth defects that may potentially occur because of this condition may include low birth weight, feeding problems and trouble reaching ” baby milestones”. Although there is currently no cure for 10p terminal deletion syndrome, there are various resources to help manage the condition and treat birth defects. Doctors seek help from various therapists and community services to provide support and care for families affected by chromosome 10p terminal deletion syndrome.

Connect. Empower. Inspire.