Congenital Muscular Dystrophy Diseases are diseases that should be followed up by a team of doctors with a multidisciplinary approach and under the supervision of a pediatric neurologist. Since there is no cure for these diseases yet, early diagnosis, recognition of the disease, proactive treatments for symptoms and strict follow-up of the disease are important.
Disease symptoms may vary depending on the mutation and subtype in the causative gene. Not all symptoms can be seen in all patients. The family of the patient needs to be informed on many issues.