Stages and Symptoms of Spinal Muscular Atrophy
Spinal muscular atrophy (SMA) is a genetic disorder that causes weakness and dissipation of muscles. It is a common genetic disorder, affecting one in every 6,000 to 10,000 babies worldwide and is rarely found in adults. Doctors believe that the inadequate production of protein in the body causes this condition. Here are the stages and symptoms of spinal muscular atrophy. Type 0 SMA Type 0 SMA occurs in the womb, even before the child is born. Poor fetal movement, inability to breathe, move or swallow, severe weakness, and joint deformities are some of the symptoms of this type of SMA. Infants suffering from this type do not develop proper motor skills. Type 1 SMA This type is also known as Werdnig-Hoffmann Disease or infantile-onset spinal muscular atrophy. It is the most common and also considered as the most severe type of SMA. The symptoms can be clearly seen at birth or in the first six months. Children suffering from this type of SMA are unable to sit or stand. Symptoms of Type 1 SMA are reduced muscle tone, limited ability to move, lack of reflexes, tremors, respiratory infections, and difficulty in sucking, swallowing, and breathing. Some children also have scoliosis and other skeletal issues.