Dystrophy refers to a group of disorders characterized by the progressive degeneration or weakening of tissues within the body. Muscular dystrophy, for example, is a genetic condition that leads to the gradual deterioration of muscle tissue and weakness over time. There are various types of muscular dystrophy, each with its own specific genetic mutation and pattern of muscle ... 【More】
Dystrophy refers to a group of disorders characterized by the progressive degeneration or weakening of tissues within the body. Muscular dystrophy, for example, is a genetic condition that leads to the gradual deterioration of muscle tissue and weakness over time. There are various types of muscular dystrophy, each with its own specific genetic mutation and pattern of muscle involvement. Other types of dystrophy affect different tissues, such as the nervous system, bones, or connective tissues. Symptoms of dystrophy may include muscle weakness, loss of muscle mass, difficulty walking or moving, joint stiffness, and in some cases, organ dysfunction. Treatment for dystrophy typically focuses on managing symptoms, slowing disease progression, and improving quality of life through physical therapy, medications, assistive devices, and supportive care. Research into genetic therapies and other innovative treatments is ongoing to provide better outcomes for individuals with dystrophy. 【Less】
Lattice Corneal Dystrophy Type I: Lifestyle Tips disease
Corneal Dystrophy, Lattice Type I, also known as lattice corneal dystrophy type i, is related to corneal dystrophy and lattice corneal dystrophy. An important gene associated with Corneal Dystrophy, Lattice Type I is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways is Coregulation of Androgen ...
Living with Granular Corneal Dystrophy Type 1 disease
Corneal Dystrophy, Groenouw Type I, also known as cdgg1, is related to corneal dystrophy and corneal dystrophy, reis-bucklers type. An important gene associated with Corneal Dystrophy, Groenouw Type I is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways are Keratan sulfate biosynthesis and ...
Elevating Quality of Life for Bietti Dystrophy Patients disease
Bietti Crystalline Corneoretinal Dystrophy, also known as bietti crystalline dystrophy, is related to scotoma and progressive cone dystrophy. An important gene associated with Bietti Crystalline Corneoretinal Dystrophy is CYP4V2 (Cytochrome P450 Family 4 Subfamily V Member 2), and among its related pathways/superpathways are Fatty acid ...
LMNA-CMD: Symptoms, Care, and Lifestyle disease
Muscular Dystrophy, Congenital, Lmna-Related, also known as congenital muscular dystrophy, is related to congenital muscular dystrophy-dystroglycanopathy a14 and congenital muscular dystrophy-dystroglycanopathy type a5. An important gene associated with Muscular Dystrophy, Congenital, Lmna-Related is LMNA (Lamin A/C), and among its related ...