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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
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- Deficiency
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Information for Muscular dystrophy, progressive
- Clinical Manifestations
- Signs & Symptoms
- Slow eating pattern
- Glossoptosis/Swallowing tongue
- Flabby muscles
- Gowers sign positive
- Head Lag Infant Sign
- Hypotonia
- Muscle Atrophy
- Muscle weakness
- Neck weakness/head nodding
- Proximal symmetrical muscle weakness
- Symmetrical muscle involvement/stiffness
- Unable to stand up from sitting position
- Weak/Weak as a kitten (symptom)
- Weakness climbing stairs
- Weakness, legs, bilateral
- Head Neck Floppy Infant Hypotonia Sign
- Hyporeflexia/DTRs decreased
- Limb weakness/signs
- Weak lower extremities
- Weakness/Diffuse motor loss
- Child won't walk
- Urine Incontinence
- Balance problems
- Difficulty climbing stairs
- Enervated/extreme acute fatigue
- Falling
- Muscle Wasting/Diffuse
- Unable to stand
- Weakness
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Laboratory Tests
- Abnormal Lab Findings - Decreased
- URINE 17-Ketosteroids
- URINE Hydroxyproline
- Abnormal Lab Findings - Increased
- Aldolase, serum (Lab)
- Aspartamine aminotransferase (SGOT, AST) (Lab)
- CPK/CK/Creatine kinase/Creatine phosphokinase (Lab)
- Lactic Dehydrogenase (LDH LH) (Lab)
- URINE Catecholamines
- URINE Creatine
- URINE Metanephrines
- URINE Ribose
- Diagnostic Test Results
- Other Tests & Procedures
- PFT/Forced vital capacity decreased
- Pathology
- BX/Muscle Biopsy Abnormal
- BX/Muscle biopsy/Fiber atrophy
- BX/Muscle biopsy/Increased interstitial tissue
- BX/Muscle/Non-uniform fiber size
- Electrodiagnosis
- EMG/Abnormal findings
- EMG/Muscular Dystrophic signs
- X-RAY With contrast
- Barium Swallowing Cine Abnormality
- Associated Diseases & Rule outs
- Rule Outs
- Dermatomyositis
- Polymyositis
- Walker Warburg Syndrome
- Associated Disease & Complications
- Alveolar hypoventilation/extrapulmonary
- Cardiomyopathy
- Hypoventilation, alveolar
- Lateral scoliosis/Rotosclerosis
- Muscular dystrophy
- Neonatal Hypotonia/Floppy Baby Syndrome
- Scoliosis
- Ineffective Cough or Reflex
- Disease Mechanism & Classification
- Class
- CLASS/Motor neuron/unit disorder (ex)
- CLASS/Muscle disorder (ex)
- CLASS/Muscle/tendon/extremities (category)
- CLASS/Striated muscle disorder (ex)
- Pathophysiology
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Absent Dystrophin muscle cells
- Pathophysiology/Lung Hypoventilation
- Pathophysiology/Lung Ventilation Mechanics
- Process
- PROCESS/Hereditofamilial (category)
- PROCESS/Use/Age/atrophic disorder (category)
- PROCESS/Muscular dystrophy disorder (ex)
- Treatment
- Other Treatments
- TX/Physical therapy
- Definition
- Be the first to add a definition for Muscular dystrophy, progressive
- External Links Related to Muscular dystrophy, progressive
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)
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