Congenital muscular dystrophy without intellectual disability (CMD-ID) is a rare form of muscular dystrophy that affects the muscles and does not cause intellectual disability. It is caused by a genetic mutation that affects the production of proteins needed for muscle development and maintenance. Symptoms of CMD-ID include muscle weakness, joint contractures, and muscle wasting. Treatment typically involves physical therapy, occupational therapy, and medications to help manage symptoms.

The symptoms of Congenital Muscular Dystrophy (CMD) without Intellectual disability can vary depending on the type of CMD, but may include:

-Delayed motor development
-Muscle weakness
-Joint contractures
-Muscle wasting
-Difficulty walking
-Difficulty with fine motor skills
-Scoliosis
-Cardiomyopathy
-Respiratory problems
-Gastrointestinal problems
-Feeding difficulties
-Seizures
-Visual impairment
-Hearing impairment
-Skeletal deformities

1. Mutations in the genes that code for proteins involved in muscle formation and maintenance.
2. Mutations in the genes that code for proteins involved in the formation of the nervous system.
3. Mutations in the genes that code for proteins involved in the formation of the connective tissue.
4. Mutations in the genes that code for proteins involved in the formation of the skeletal system.
5. Mutations in the genes that code for proteins involved in the formation of the circulatory system.
6. Mutations in the genes that code for proteins involved in the formation of the immune system.
7. Mutations in the genes that code for proteins involved in the formation of the endocrine system.
8. Mutations in the genes that code for proteins involved in the formation of the digestive system.
9. Mutations in

1. Physical therapy: Physical therapy is an important part of treatment for congenital muscular dystrophy without intellectual disability. Physical therapy can help improve strength, flexibility, balance, and coordination.

2. Occupational therapy: Occupational therapy can help people with congenital muscular dystrophy without intellectual disability learn how to use assistive devices, such as wheelchairs, walkers, and canes. It can also help them learn how to perform daily activities, such as dressing, bathing, and eating.

3. Speech therapy: Speech therapy can help people with congenital muscular dystrophy without intellectual disability learn how to communicate more effectively.

4. Medications: Medications can help reduce muscle spasms and improve muscle strength.

5. Surgery: Surgery may be recommended in some cases to help improve mobility and reduce pain.

1. Genetic mutations: Mutations in the genes responsible for producing proteins that are essential for muscle development can cause congenital muscular dystrophy without intellectual disability.

2. Family history: A family history of congenital muscular dystrophy increases the risk of developing the condition.

3. Gender: Males are more likely to be affected by congenital muscular dystrophy without intellectual disability than females.

4. Age: Congenital muscular dystrophy without intellectual disability is more common in infants and young children.

5. Ethnicity: Congenital muscular dystrophy without intellectual disability is more common in certain ethnic groups, such as those of European descent.

At this time, there is no cure for congenital muscular dystrophy without intellectual disability. However, there are medications and treatments available to help manage the symptoms of the condition. These include physical therapy, occupational therapy, speech therapy, and medications to help with muscle spasms, pain, and other symptoms.