Dystrophy, muscular

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Dystrophy, muscular

Dystrophy, muscular

One of a group of genetic diseases characterized by progressive weakness and degeneration of the skeletal or voluntary muscles which control movement. The muscles of the heart and some other involuntary muscles are also affected in some forms of muscular dystrophy, and a few forms involve other organs as well. The major forms of muscular dystrophy include: Duchenne muscular dystrophy; Becker muscular dystrophy; limb-girdle muscular dystrophy; facioscapulohumeral muscular dystrophy; congenital muscular dystrophy; oculopharyngeal muscular dystrophy; distal muscular dystrophy; Emery-Dreifuss muscular dystrophy and myotonic dystrophy. Muscular dystrophy can affect people of all ages. Although some forms first become apparent in infancy or childhood, others may not appear until middle age or later. Duchenne muscular dystrophy is the most common kind of muscular dystrophy affecting children. Myotonic dystrophy is the most common of these diseases in adults.

RELATED TERMS
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Genetic
Hereditary. Having to do with the genes.

Heart
The hollow, muscular organ responsible for pumping blood through the circulatory system.

Dystrophy
Partial atrophy of tissue or an organ as a result of imperfect cell nutrition.

Congenital
Present at birth.

Distal
A location farther from a point of reference. For example, the foot is distal to the knee, relative to the center of the body.

Affect
This word is used to described observable behavior that represents the expression of a subjectively experienced feeling state (emotion). Common examples of affect are sadness, fear, joy, and anger. The normal range of expressed affect varies considerably between different cultures and even within the same culture. Types of affect include: euthymic, irritable, constricted; blunted; flat; inappropriate, and labile.

Infancy
Babyhood; the period of development between birth and the beginning of early childhood between the ages of two and three years.

Childhood
1. The time for a boy or girl from birth until he or she is an adult. 2. The more circumscribed period of time from infancy to the onset of puberty.

SIMILAR TERMS
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Dysthymia
A type of depression involving long-term, chronic symptoms that are not disabling, but keep a person from functioning at "full steam" or from feeling good. Dysthymia is a less severe type of depression than what is accorded the diagnosis of major depression. However, people with dysthymia may also sometimes experience major depressive episodes, suggesting that there is a continuum between dysthymia and major depression.

Dystocia
When labor does not progress. Uterine dystocia is when contractions donot intensify; shoulder dystocia is when a baby's

Dystocia, fetal
Dystocia caused by the fetus due to its size (too big), shape or position in the uterus.

Dystonia
Dystonia is a neurological movement disorder with involuntary muscle contractions, forcing specific parts of the body into abnormal movements or positions, sometimes causing pain.

Dystonia musculorum deformans (DMD)
Also called torsion dystonia, this is a fortunately rare, generalized dystonia (a state of abnormal -- either excessive of inadequate -- muscle tone) that can be inherited, usually begins in childhood, and becomes progressively worse. It can leave individuals seriously disabled and confined to a wheelchair.

Dystonia, dopa-responsive (DRD)
A condition that typically begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity and can be successfully treated with drugs. Segawa dystonia is an important variant of DRD. In Segawa dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasing disability in the afternoon and evening and after exercise. DRD may not only be rare but also rarely diagnosed since it mimics some forms of cerebral palsy.

Dystonia, idiopathic torsion
A form of dystonia known as early-onset torsion dystonia (also called generalized torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating.

Dystonia, oromandibular
Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult.

Dystonia, Segawa
An important variant form of dopa-responsive dystonia (DRD). DRD typically begins in childhood or adolescence with progressive difficulty in walking and, in some cases, with spasticity. DRD, by definition, can be successfully treated with dopa. In Segawa dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening and after exercise.

Dystonia, torsion
A form of dystonia known as early-onset torsion dystonia (also called idiopathic or generalized torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. Most children with the disorder are unable to perform the simplest of motor tasks and are confined to a wheelchair by the time they reach adulthood.

Dystopia
Displacement.

Dystrophic epidermolysis bullosa
A blistering skin condition inherited in both autosomal dominant and recessive manners and in which the filaments that anchor the epidermis to the underlying dermis are either absent or do not function. This is due to defects in the gene for type VII collagen, a fibrous protein that is the main component of the anchoring filaments.

Dystrophin
A protein, a chemical substance made by muscle fibers.

Dystrophy
Partial atrophy of tissue or an organ as a result of imperfect cell nutrition.

Dystrophy, autoimmune polyendocrinopathy
Dystrophy, autoimmune polyendocrinopathy-candidiasis-ectodermal (APECED) is a genetic autoimmune disease with an extraordinary array of clinical features but characterized most often by at least 2 of the following 3 findings: hypoparathyroidism -- underfunction of the parathyroid glands which control calcium, candidiasis (yeast infection), and adrenal insufficiency (underfunction of the adrenal gland). APECED was the first systemic (bodywide) autoimmune disease found due to a defect in a single gene.

Dystrophy, cone
A disease of the cones, the specialized light-sensitive cells that act as photoreceptors in the retina of the eye, providing sharp central vision and color vision. The cone dystrophies are a form of genetic macular degeneration characterized by progressive deterioration of the cones that leads to the distinctive triad of loss of color vision, photophobia, and reduced central vision. Cone dystrophy genes have been mapped to chromosome regions 6p21.1, 6q25-q26, 17p12-13, and Xp21.1-p11.3. In region 6p21.1, mutations have been found in the gene that encodes GCAP1, a key component in the recovery of photoreceptor cells to the dark-adapted state after exposure to a light stimulus.

Dystrophy, myotonic
An inherited disease in which the muscles contract but have decreasing power to relax -- this phenomenon is termed myotonia (irritability and prolonged contraction of muscles). The disease also produces leads to a mask-like expressionless face, premature balding, cataracts, and heart arrhythmias (abnormalities in heart rhythm). The onset of such problems is usually in young adulthood. However, onset can be at any age and the disease is extremely variable in the degree of severity.

PREVIOUS AND NEXT TERMS
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Dystonia, Segawa
An important variant form of dopa-responsive dystonia (DRD). DRD typically begins in childhood or adolescence with progressive difficulty in walking and, in some cases, with spasticity. DRD, by definition, can be successfully treated with dopa. In Segawa dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening and after exercise.

Dystonia, torsion
A form of dystonia known as early-onset torsion dystonia (also called idiopathic or generalized torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. Most children with the disorder are unable to perform the simplest of motor tasks and are confined to a wheelchair by the time they reach adulthood.

Dystrophic epidermolysis bullosa
A blistering skin condition inherited in both autosomal dominant and recessive manners and in which the filaments that anchor the epidermis to the underlying dermis are either absent or do not function. This is due to defects in the gene for type VII collagen, a fibrous protein that is the main component of the anchoring filaments.

Dystrophy, autoimmune polyendocrinopathy
Dystrophy, autoimmune polyendocrinopathy-candidiasis-ectodermal (APECED) is a genetic autoimmune disease with an extraordinary array of clinical features but characterized most often by at least 2 of the following 3 findings: hypoparathyroidism -- underfunction of the parathyroid glands which control calcium, candidiasis (yeast infection), and adrenal insufficiency (underfunction of the adrenal gland). APECED was the first systemic (bodywide) autoimmune disease found due to a defect in a single gene.

Dystrophy, cone
A disease of the cones, the specialized light-sensitive cells that act as photoreceptors in the retina of the eye, providing sharp central vision and color vision. The cone dystrophies are a form of genetic macular degeneration characterized by progressive deterioration of the cones that leads to the distinctive triad of loss of color vision, photophobia, and reduced central vision. Cone dystrophy genes have been mapped to chromosome regions 6p21.1, 6q25-q26, 17p12-13, and Xp21.1-p11.3. In region 6p21.1, mutations have been found in the gene that encodes GCAP1, a key component in the recovery of photoreceptor cells to the dark-adapted state after exposure to a light stimulus.

Dystrophy, muscular

Dystrophy, myotonic
An inherited disease in which the muscles contract but have decreasing power to relax -- this phenomenon is termed myotonia (irritability and prolonged contraction of muscles). The disease also produces leads to a mask-like expressionless face, premature balding, cataracts, and heart arrhythmias (abnormalities in heart rhythm). The onset of such problems is usually in young adulthood. However, onset can be at any age and the disease is extremely variable in the degree of severity.

Dysuria
Painful or difficult urination. This includes burning on urination. Dysuria is most commonly due to bacterial infection of the urinary tract causing inflammation of the bladder (cystitis) or kidney (pyelonephritis). In women, dysuria may also reflect inflammation of the vagina (vaginitis) or vulva (vulvitis). And in men, dysuria may be due to inflammation of the prostate (prostatitis) or the urethra (urethritis) from gonorrhea or chlamydia.

Danish doctor
A doctor who, being or not a citizen of that country, has been admitted to practice medicine in Denmark.

Downunder doctor
A doctor who, being or not a citizen of that country, has been admitted to practice medicine in Australia or New Zealand.

Dutch doctor
A doctor who, being or not a citizen of that country, has been admitted to practice medicine in the Netherlands.

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This dictionary contains 25007 terms.

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