Spinal Muscular Atrophy Type 2

Spinal Muscular Atrophy Type 2 (also known as "spinal muscular atropy type II") is an autosomal recessive disease and is a form of spinal muscular atrophy (SMA).

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Symptoms

Children with spinal muscular atrophy type 2 manifest less severe weakness than children with Werdnig-Hoffman disease. Symptoms are usually noticed later in life, usually between the age of 6 to 18 months. The clinical features are similar to those found in children with Type 1; in fact, there are many children for whom the characterization of Type 1 (Werdnig-Hoffman) or Type 2 SMA becomes a "best guess". Children with Type 2 SMA usually achieve the ability to sit independently, however, they almost never achieve the ability to walk or stand without support.

Prognosis

Some children with SMA Type 2 have a relatively static course and remain free of life threatening complications such as pneumonia. Other children, have progressive weakness of their swallowing and respiratory muscles. Many youngsters with SMA Type 2 develop curvature of the spine (Kyphoscoliosis) and other orthopedic problems. Skillful management by a team of physical therapists and orthopedic surgeons is usually needed to manage these problems.

See also

• Motor neurone disease
• Spinal Muscular Atrophy
• Kugelberg-Welander disease
• Werdnig-Hoffman disease

Source

• Fight SMA Spinal Muscular Atrophy Guidebook