Congenital Muscular Dystrophy (CMD): What It Is & Symptoms
Congenital muscular dystrophy (CMD) is a group of rare muscular dystrophies that cause muscle weakness in infants. There are several different subtypes based on which gene has a mutation. Treatment involves managing symptoms with various strategies, like physical therapy, assistive devices and medications.
Congenital Muscular Dystrophy (CMD) - Diseases | Muscular Dystrophy ...
What is congenital muscular dystrophy (CMD)? Congenital muscular dystrophy (CMD) refers to a group of muscular dystrophies that become apparent at or near birth. Muscular dystrophies in general are genetic, degenerative diseases primarily affecting voluntary muscles.
Congenital Muscular Dystrophy - StatPearls - NCBI Bookshelf
2023年7月3日 · Congenital muscular dystrophy is one of the variants of muscle weakness disorders presenting early in life during infancy and soon after birth. The difference between congenital myopathies and muscular dystrophies is that dystrophies are gradually progressive and are associated with increased muscle breakdown with age.[1]
Congenital muscular dystrophy - Wikipedia
Congenital muscular dystrophies are autosomal recessively-inherited muscle diseases. They are a group of heterogeneous disorders characterized by muscle weakness which is present at birth and the different changes on muscle biopsy that ranges from myopathic to overtly dystrophic due to the age at which the biopsy takes place. [1][4]
Congenital Muscular Dystrophy - Symptoms, Causes, Treatment …
2013年5月8日 · Congenital muscular dystrophy (CMD) is a general term for a group of genetic muscle diseases that occur at birth (congenital) or early during infancy.
Congenital muscular dystrophy | About the Disease | GARD
Congenital muscular dystrophy (CMD) refers to a group of inherited conditions that affect the muscles and are present at birth or in early infancy. Common features include hypotonia; progressive muscle weakness and degeneration (atrophy); joint contractures; and delayed motor milestones (i.e. sitting up, walking, etc).
Congenital muscular dystrophy: Symptoms, causes, and more
2024年6月18日 · Congenital muscular dystrophy (CMD) is an inherited disease that affects muscles throughout the body. Most people with CMD receive a diagnosis during their birth or infancy.
Congenital Muscular Dystrophy: Causes, Prognosis, & Types
2024年6月21日 · Congenital muscular dystrophy is a group of genetic muscle diseases appearing around birth. It involves the weakening and degeneration of muscles over time. CMD can cause a lack of mobility and muscle tone, as well as difficulty …
Signs and Symptoms of Congenital Muscular Dystrophy (CMD)
The term congenital muscular dystrophy (CMD) is actually the name for a group of muscular dystrophies united by the fact that muscle weakness begins in infancy or very early childhood (typically before age 2). Congenital diseases are those in which the symptoms are present at or soon after birth.
This fact sheet is provided to help you understand the current evidence for diagnosing and managing congenital muscular dystrophy (CMD). The American Academy of Neurology (AAN) is the world’s largest association of neurologists and neuroscience professionals.