Congenital myopathy causes loss of muscle tone and muscle weakness in infancy and delayed motor skills, such as walking, later in childhood.
The main types include congenital myopathy, muscular dystrophy , inflammatory myopathy, and drug-induced myopathy.
Congenital myopathy (CM) is a term used for muscle disorders present at birth, including hundreds of distinct neuromuscular syndromes and disorders.
Four distinct disorders are classified as CMs: central core disease, nemaline rod myopathy, centronuclear (myotubular) myopathy, and multicore myopathy.
Congenital myopathies are a group of myopathies, usually present from birth, that display structural changes in the skeletal muscles. The list of diseases defined as congenital myopathies varies.
Symptoms of congenital GBS infection include breathing difficulties; shock; sepsis; pneumonia; and, meningitis.
There are a number of different symptoms of congenital heart defects, as there are many kinds of heart defects. Some common symptoms include chest pain or angina, and heart burn.
What are the chances of your offspring having myopathy if your husband's brother has myopathy?
Symptoms in the congenital form of myotonic dystrophy are evident at birth. Affected infants show muscle weakness, respiratory defects, and eventually, mental retardation
Symptoms of congenital fifth disease include bright red rash on the cheeks; lacy, red rash on the neck, trunk, and legs; joint pain; fatigue; and, malaise.
Diagnosis of congenital infections in newborns may be based on a physical examination, symptoms, and blood or urine tests.
Congenital methemoglobinemia is typically benign and should be observed. If methemoglobinemia symptoms occur the person should be taken to the hospital for treatment.
There is currently no cure for metabolic myopathy, but treatment aims to manage symptoms and improve quality of life. This may include physical therapy, medication, and lifestyle modifications. It is important to work with a healthcare team to develop a personalized treatment plan.