Disease Information for Duchenne's Muscular Dystrophy/Pseudohypertrophic
adult pseudohypertrophic muscular dystrophy, benign X linked recessive muscular dystrophy, CARDIOMYOPATHY DILATED 3B, CARDIOMYOPATHY DILATED X LINKED, Childhood Muscular Dystrophy Pseudohypertrophic, Childhood Pseudohypertrophic Muscular Dystrophy, classic X linked recessive muscular dystrophy, CMD3B, DMD, DMD Duchenne muscul dystroph, DMD Duchenne muscular dystrophy, Duchenne de Boulogne muscular dystrophy, Duchenne dystrophy, Duchenne Griesinger, Duchenne Griesinger syndrome, Duchenne motor neuron disease, Duchenne musc dyst, Duchenne muscular dystrophy, Duchenne muscular dystrophy (disorder), Duchenne muscular dystrophy (DMD), Duchenne myodystrophy, Duchenne pseudohypertrophic muscular dystrophy, Duchenne syndrome, Duchenne type dystrophy, Duchenne Type Progressive Muscular Dystrophy, Duchenne's Muscular Dystrophy, Dystrophies Pseudohypertrophic Muscular, Dystrophy Duchenne Muscular, dystrophy Duchenne type, dystrophy muscular Duchenne type, Dystrophy Pseudohypertrophic Muscular, mild X linked recessive muscular dystrophy, motor neuron Duchenne, Muscular Dystrophies Pseudohypertrophic, Muscular Dystrophy Childhood Pseudohypertrophic, MUSCULAR DYSTROPHY DUCHENNE, MUSCULAR DYSTROPHY DUCHENNE TYPE, Muscular Dystrophy Pseudohypertrophic, Muscular Dystrophy Pseudohypertrophic Childhood, MUSCULAR DYSTROPHY PSEUDOHYPERTROPHIC PROGRESSIVE DUCHENNE TYPE, progressive muscular dystrophy Duchenne type, progressive muscular dystrophy of childhood, pseudohypertrophic adult muscular dystrophy, Pseudohypertrophic Childhood Muscular Dystrophy, Pseudohypertrophic Muscular Dystrophies, Pseudohypertrophic Muscular Dystrophy, Pseudohypertrophic Muscular Dystrophy Childhood, pseudohypertrophic muscular paralysis, pseudohypertrophic progressive muscular dystrophy, pseudohypertrophic progressive muscular dystrophy Duchenne type, Pseudohypertrph musc dystrophy, Severe generalized familial muscular dystrophy, X linked dilated cardiomyopathy, X linked dilated cardiomyopathy (XLCM), X linked muscular dystrophy, X linked recessive muscular dystrophy, XLCM
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Muscular Dystrophy, Duchenne; Childhood Muscular Dystrophy; DMD; Muscular Dystrophy, Classic X-linked Recessive; Progressive Muscular Dystrophy of Childhood; Pseudohypertrophic Muscular Dystrophy; Duchenne Muscular Dystrophy, a hereditary degenerative disease of skeletal (voluntary) muscles, is considered the most prevalent form of childhood muscular dystrophy; The disorder typically is recognized from approximately age three to six years and has a relatively rapid, progressive disease course; Duchenne Muscular Dystrophy is initially characterized by muscle weakness and wasting (atrophy) within the pelvic area that may be followed by involvement of the shoulder muscles; With disease progression, muscle weakness and atrophy affect the trunk and forearms and gradually progress to involve most major muscles of the body; In individuals with the disorder, initial findings may include an unusual, waddling manner of walking (gait); difficulty climbing stairs or rising from a sitting position; and repeated falling; With disease progression, additional abnormalities may develop, such as progressive curvature of the spine; wasting of thigh muscles and abnormal enlargement of the calves due to degenerative changes of muscle fibers (pseudohypertrophy); and abnormal fixation of certain joints (joint contractures) due to muscle weakness, prolonged immobility, and shortening of muscle fibers; By approximately age 10 to 12, most affected individuals require the use of a wheelchair; Duchenne Muscular Dystrophy is also typically characterized by additional abnormalities, including involvement of heart muscle (cardiomyopathy) and varying degrees of intellectual impairment; Affected individuals may develop an increased susceptibility to respiratory infections (eg, pneumonia), respiratory failure, impaired ability of the heart to pump blood effectively (heart failure), or other serious findings, leading to potentially life-threatening complications by late adolescence or early adulthood; Duchenne Muscular Dystrophy is caused by changes (mutations) of a gene on the short arm (p) of chromosome X (Xp21_2); The gene regulates the production of a protein that is found in skeletal and cardiac muscle; Known as dystrophin, the protein is thought to play an important role in maintaining the structure of these muscle cells; In most affected individuals, Duchenne Muscular Dystrophy is inherited as an X-linked recessive trait; Therefore, the disorder is usually fully expressed in males only; However, in rare instances, females who carry a copy of the mutated gene (heterozygous carriers) may develop certain, typically milder symptoms associated with the disorder; In addition, for some individuals with Duchenne Muscular Dystrophy, there is no family history of the disease; In such cases, the disorder may be caused by new (sporadic) genetic mutations that occur for unknown reasons---------[NORD 2005]--------
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Demographics & Risk Factors[next]
- Population Group
- Population/Pediatrics population
- Family History
- Sex & Age Groups
- Population/Adult/all
- Population/Boy patient
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population/Male
- Population/Twenties-Adult/male
- Population Group
Clinical Manifestations[previous][top][next]
- Typical Clinical Presentation
- Males sicker than females/characteristic
- Presentation/Congestive heart failure/child
- Presentation/Recurrent respiratory infections
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Course/Life-span decreased
- Course/Progressive
- Course/Progressive/slowly chronic illness
- Onset/1-5 years old
- Onset/5-15 years old
- Onset/age 5
- Onset/Childhood
- Onset/Infancy
- Onset/Young adult
- Signs & Symptoms
- Child
- Dysphagia/liquids
- Dysphagia/progressive
- Dysphagia/Swallowing difficulties
- Weight loss in Children
- Tongue fasciculations
- Tongue muscle atrophy
- Calf enlargement/bilateral
- Flabby muscles
- Hypertrophy leg muscles
- Hypotonia
- Muscle atrophy/wasting
- Muscle tone/decreased
- Muscle weakness
- Muscles swelling
- Neck weakness/head nodding
- Pelvic/limb girdle weakness/bilateral
- Proximal muscle weakness
- Pseudohypertrophy calf muscle/sign
- Shoulder/limb girdle weakness/bilateral
- Thigh muscle atrophy
- Unable to stand up from sitting position
- Weak/Weak as a kitten (symptom)
- Weakness climbing stairs
- Weakness, legs, bilateral
- Delayed speech/language development
- Dysarthria
- Hyporeflexia/DTRs decreased
- Limb weakness/signs
- Poor head control/infant
- Unable to walk
- Waddling gait
- Weak lower extremities
- Weakness/Diffuse motor loss
- Dyspnea
- Hypoventilation/sign
- Respiratory excursions decreased
- Shallow breathing
- Difficulty learning/school/workplace
- Decreased ankle range of motion
- Limp
- Lumbar lordosis/excess
- Delayed speech development/impediment
- Speech disturbance/motor
- Difficulty climbing stairs
- Difficulty rising from chair
- Enervated/extreme acute fatigue
- Unable to stand
- Walking difficulties
- Weakness
- Wheelchair bound
- Typical Clinical Presentation
Laboratory Tests[previous][top][next]
- Abnormal Lab Findings (Non Measured)
- Abnormal Lab Findings - Increased
Diagnostic Test Results[previous][top][next]
- Pathology
- Electrodiagnosis
- EKG (ECG)
- X-RAY
Associated Diseases & Rule outs[previous][top][next]
- Rule Outs
- Associated Disease & Complications
- Acute respiratory failure/Respiratory arrest
- Ankle contracture
- Atelectasis, pulmonary
- Becker's muscular dystrophy/Pseudohypertrophic
- Cardiac arrhythmias
- Cardiomyopathy
- Congestive heart failure
- Duchenne muscular dystrophy/Pseudohypertrophic
- Dyslexia
- Joint contractures
- Kyphoscoliosis
- Mental retardation
- Mitral valve prolapse syndrome
- Muscular dystrophy
- Obstructive sleep apnea/Children
- Paraparesis
- Pneumonia, aspiration
- Pneumonia, bacterial
- Pneumonia/Bronchopneumonia
- Respiratory muscle weakness
- Rhabdomyolysis
- Scoliosis
- Tendon contracture, Achilles
- Heart Failure in a Child
Disease Mechanism & Classification[previous][top][next]
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Motor neuron/unit disorder (ex)
- CLASS/Muscle disorder (ex)
- CLASS/Muscle/tendon/extremities (category)
- CLASS/Striated muscle disorder (ex)
- Pathophysiology
- Pathophysiology/Chromosome/gene/Duetan colorblind loc
- Pathophysiology/Dystrophin Gene Mutation
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Gene locus Chromosome Xp
- Pathophysiology/Gene locus Xp21.2
- Pathophysiology/Gene locus Xp21.3
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Maternal inheritance
- Pathophysiology/Absent Dystrophin muscle cells
- Pathophysiology/Defective dystrophin muscle cells
- Pathophysiology/Motor nuclei medulla/pons
- Pathophysiology/Skeletal defomities/acquired
- Process
- PROCESS/Degenerative/necrosis disorder (category)
- PROCESS/Developmental/delayed expression disorder (ex)
- PROCESS/Disease with two subtypes
- PROCESS/Dystrophic disorder (ex)
- PROCESS/Eponymic (category)
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
- PROCESS/Hereditofamilial (category)
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
- PROCESS/Use/Age/atrophic disorder (category)
- PROCESS/Muscular dystrophy disorder (ex)
- Class
-
- Synonym
- Synonym/Becker muscular dystrophy
- Synonym/Becker pseudohypertrophic muscular dystrophy
- Synonym/Classic X-linked recessive muscular dystrophy
- Synonym/Duchenne de Boulogne muscular dystrophy
- Synonym/Duchenne/Becker muscular dystrophy
- Synonym/Duchenne-Griesinger syndrome
- Synonym/Duchenne's muscular dystrophy, late type
- Synonym/Muscular dystrophy, pseudohypertrophic/childhood
- Synonym/Muscular dystrophy, slowly progressive
- Synonym/Muscular dystrophy/Pseudohypertrophic
- Synonym/Progressive muscular dystrophy, Duchenne type
- Synonym
External Links Related to Duchenne's Muscular Dystrophy/Pseudohypertrophic[previous][top]
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