50 Facts About Werdnig–Hoffmann Disease
Werdnig – Hoffmann Disease , also know asSpinal Muscular Atrophy Type 1 ( SMA Type 1 ) , is a grievous genetic upset that affects muscle movement . This condition is due to a mutation in theSMN1 factor , result to the departure of motor neurons in the spinal electric cord and brainstem . Babies with this disease often show symptoms like muscle failing , poor heftiness tone , and difficulty take a breather or swallow ....