Chromosome 1, Monosomy 1p22 p13

Overview

Type of disease: Rare conditions

Chromosome 1, monosomy 1p22 p13 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 hand defects or short stature, as well as intellectual disabilities and hearing loss. Although there is currently no cure for Chromosome 1, monosomy 1p22 p13, 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, monosomy 1p22 p13.

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