Chromosome 12p Partial Deletion

Overview

Type of disease: Rare conditions

Chromosome 12p partial deletion syndrome 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 short stature, short and webbed neck, or broad thumbs, as well as intellectual disabilities. Although there is currently no cure for chromosome 12p partial 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 12p partial deletion syndrome.

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