Inclusion body myopathy- 2 autosomal recessive
Overview
Inclusion body myopathy, 2 autosomal recessive: A very rare, recessively inherited genetic disorder involving progressive muscle weakness and wasting in the arms and legs. The distinctive feature of this particular disorder is the fact that the thigh muscles are usually spared.
Symptoms
The list of signs and symptoms mentioned in various sources for Inclusion body myopathy, 2 autosomal recessive includes the 9 symptoms listed below: * Arm muscle weakness * Shoulder girdle muscle weakness * Leg muscle weakness * Pelvic girdle muscle weakness * Arm muscle wasting * Shoulder girdle muscle wasting * Leg muscle wasting * Pelvic girdle muscle wasting * Walking difficult
Causes
Leg muscle wasting
Prognosis
Prognosis of Inclusion body myopathy, 2 autosomal recessive: severe disability usually occurs in 10 to 20 years.The 'prognosis' of Inclusion body myopathy, 2 autosomal recessive usually refers to the likely outcome of Inclusion body myopathy, 2 autosomal recessive. The prognosis of Inclusion body myopathy, 2 autosomal recessive may include the duration of Inclusion body myopathy, 2 autosomal recessive, chances of complications of Inclusion body myopathy, 2 autosomal recessive, probable outcomes, prospects for recovery, recovery period for Inclusion body myopathy, 2 autosomal recessive, survival rates, death rates, and other outcome possibilities in the overall prognosis of Inclusion body myopathy, 2 autosomal recessive. Naturally, such forecast issues are by their nature unpredictable.