Chromosome 1, Trisomy 1q32 qter
Type of disease: Rare conditions
Chromosome 1, trisomy 1q32 qter, also known as duplication 1q32 qter, is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This can cause birth defects such as facial anomalies, finger and toe deformities, or heart defects, as well as intellectual disability. Although there is currently no cure for chromosome 1, trisomy 1q32 qter, 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 1, trisomy 1q32 qter.