3 steps to make life with distal spinal muscular atrophy type 1 manageable
Distal spinal muscular atrophy type 1 is an ailment that has no permanent cure. It is an inherited condition that begins in infancy and is characterized by muscle weakness that ultimately results in respiratory failure. Distal spinal muscular atrophy type 1 is often diagnosed between the ages of six weeks and six months; the child diagnosed with this condition, unfortunately, doesn’t survive for more than two years owing to the respiratory issues it faces.