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Disease Comparison Results (show all mode) for Duchenne's Muscular Dystrophy/Pseudohypertrophic and Mastocytosis, systemic

Clinical
Demographics
Lab
Diagnostic
Diseases
Classification
Synonyms
Treatment
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Found: 286 | Differences: 275

Duchenne's Muscular Dystrophy/Pseudohypertrophic

Found: 175 | Differences: 164

Duchenne's Muscular Dystrophy/Pseudohypertrophic and Mastocytosis, systemic sharing 11 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Signs of Poor Perfusion
Signs & Symptoms: Alcohol Trigger Deliterious; Edema Children; Plethora/Red face/Ruddy look; Bilateral ankle swelling; Bilateral leg edema/swelling; Low Blood Pressure; Signs of Poor Perfusion; Alcohol induced Flushing; Darier's sign/hive with scratch/papule; Erythematous generalized rash; Excoriations; Facial erythema; Facial flushing/Beet red; Flushing; Itching after hot bath; Macular rash; Mucocutaneous Lesions; Mucocutaneous rash/signs; Nodular rash; Pigmentation Lesions on Healing; Pigmented patches/skin; Pruritic/itching rash; Pruritis Itching; Rash; Rash, chronic/Dermatitis; Rash, macular/maculopapular or morbilliform; Telangiectasias, skin; Urticaria, nonallergic/symptomatic; Vesicular rash; Abdominal Pain; Abdominal Pain Crampy; Abdominal pain/triggered by alcohol; Acute Diarrhea; Acute Diarrhea in Children; Bowel Habit Change; Chronic Diarrhea in a Child; Diarrhea; Diarrhea and Weight Loss; Diarrhea in Children; Diarrhea, chronic; Diarrhea, explosive; Diarrhea, recurrent; Dyspepsia; Epigastric Pain; Epigastric recurrent pain attacks; Fatty food intolerance; Heartburn/Pyrosis; Nausea; Peptic ulcer like pain; Specific food/intolerance; Upper Abdominal Pain; Vomiting; Weight loss in Children; Lymphadenopathy; Lymphadenopathy Systemic; Hepatosplenomegaly; Palpable Liver/Hepatomegaly; Edema of Lower Extremities; Weak/Weak as a kitten (symptom); Confusion/Disoriented; Headache; Headache worse with valsalva/Bowel movement; Headache, throbbing, vascular; Irritability/short tempered; Bronchospasm signs; Respiratory distress; Wheezing; Mood swings/changes; Volatility/wild mood swings; Arthralgias Polyarthralgias; Bone Pain Triggered by Alcohol; Bone Pains; Joint Pains; Joint pains Arthralgias in Children; Nasal mucosal involvement/irritation; Splenomegaly; Adults sicker than children; Alcohol triggered localized pain; Certain drugs trigger rash/flushing/itch; Chronically ill patient/signs; Collapse/Prostration; Enervated/extreme acute fatigue; Episodic symptoms/events; Malaise; Neonatal edema/anasarca; Spells/Episodes of weakness; Weakness; Weakness non-neuromuscular/systemic; Weight Loss
Clinical Presentation & Variations: Presentation/Flushing Burning Ears Fingertips Periodic; Presentation/ Papular Rash Face Upper Arms
Disease Progression: Course/Chronic disease crisis/flare/attacks; Course/Chronic only; Pancytopenia with Infiltrated Marrow

Demographics & Risk Factors
Ethnic or Racial Factors: Population Caucasian/White
Past History: Past History/Peptic ulcer disease
Population Group: Child; Infant; Population/Pediatrics population
Sex & Age Groups: Population/Adult/all; Population/Child; Population/Children/all; Population/Infant

Laboratory Tests
Abnormal Lab Findings (Non Measured): Chromosomal abnormality (Lab)
Abnormal Lab Findings - Decreased: WBC; Cholesterol (Lab); Complement (total CH50) level (Lab); Hematocrit (Lab); Hemoglobin (Lab); Neutrophiles (Lab); Platelet count (Lab); RBC/Red Blood Count (Lab); WBC/White Blood Cell Count/Leukocytes (Lab)
Abnormal Lab Findings - Increased: Alkaline phosphatase, serum (Lab); Alpha Tryptase, Serum (Lab); Beta Tryptase, Serum (Lab); CarboxyPeptidase A (CPA); GASTRIC Hydrochloric acid; Heparin serum level/intrinsic (Lab); Histamine (Lab); Mast cells/peripheral blood smear (Lab); Plasma mast cell tryptase (Lab); Prostaglandin D2 serum (Lab); PT -Prothrombin time (Lab); Tryptase, serum (Lab); URINE 1,4 methyl Imidazolacetic acid; URINE Histamine; URINE Histamine metabolites; URINE N-Methylhistamine (NMH); URINE Prostaglandin D2 metabolites

Diagnostic Test Results
Other Tests & Procedures: Gastroscopy/Abnormal
Pathology: BX/Skin biopsy/Abnormal; BX/Skin Mast cells/clustered; Bone Marrow Tap/Normal; Bone Marrow/Abnormal; Bone Marrow/Mast cell infiltration; BX/Bone Marrow Biopsy/Abnormal; BX/Bone marrow focal aggregates spindle shaped mast cells; BX/Intestinal biopsy/ileum/ abnormal; BX/Intestinal biopsy/Jejunal/Abnormal; BX/Jejunal flattened/blunt villi; PATH/CNS/Reticulum system/disseminated lesions; PATH/Chloroacetate Esterase Positive stain; PATH/Tissue histamine levels very high; PATH/Mast cell tissue infiltrates
Isotope Scan: Isotope/Bone scan abnormality
CT Scan: CT/Bone Mineral Density/Increased; CT/Dexa-Scan Bone density Abnormal
X-RAY: Xray/Anomalous rib cage/congenital; Xray/Bone lesions, multiple 'punched out'; Xray/Bone perisosteal thickening/sclerosis; Xray/Bone trabecular coarsening; Xray/Increased bone density; Xray/Osteosclerosis areas/Skeletal; Xray/Pelvis bone abnormalities; Xray/Ribs Abnormal/Deformities; Xray/Skeletal findings; Xray/Skull abnormality; Xray/Spine Abnormal; Xray/Vertebrae, dense and sclerotic
X-RAY With contrast: SBS/Mucosal destruction small bowel (Xray); SBS/Mucosal folds thickened, intestinal (Xray); SBS/Multiple intramural/bowel wall small nodules (Xray); SBS/Multiple nodules/intestinal (Xray); SBS/Valvulae conniventes thickened (Xray); UGI/Duodenum distal ulcer; UGI/Duodenum thickened folds

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: Acne rosacea; Anaphylaxis, generalized; Anemia; Angioedema/angioneurotic edema; Carcinoid syndrome/metastatic carcinoid; Shock; Whipple's disease
Associated Disease & Complications - Causes: Anaphylaxis, generalized; Angioedema/angioneurotic edema; Ascites; Bee Sting Allergy; Cachexia/inanition/wasting; Chronic hives/urticaria; Cirrhosis; Depression; Dermatographism (Darier's Sign); Disulfiram-like drug reaction/alcohol; Duodenal ulcer; Eczema; Edema; Edema of newborn; Food allergy; Granulocytopenia/Neutropenia; Hyperpigmentation; Hypotension; Leukemia; Malabsorption/Steatorrhea syndrome; Male osteoporosis syndrome; Mast cell malignancy/leukemia; Mastocytosis, systemic; Migraine headache syndrome; Myeloproliferative disorder; Neonatal Erythroderma; Osteoporosis/osteopenia; Pancytopenia; Pathologic fractures; Peptic ulcer disease; Peritoneal Effusion; Pityriasis lichenoid chronicus; Portal hypertension; Rib anomalies/Hypoplastic/deformed; Shock; Skeletal dysplasia; Telangiectasia; Thoracic deformity/congenital; Urticaria pigmentosa; Urticaria/hives; Vascular headache; Kounis syndrome/Allergic Coronary Spasm; Upper GI bleeding; Metabolic Bone Disease
Disease Synergy: Synergy/Aspirin drug; Synergy/Exercise/severe; Synergy/General stress; Synergy/Infection; Synergy/Opiate administration; Synergy/Stress/Anxiety

Disease Mechanism & Classification
Class: CLASS/Pediatric disorders (ex); CLASS/Primary organ/system disorder (ex); CLASS/Soft Tissue Involvement; CLASS/Hematologic (category); CLASS/Leukocyte involvement/disorder (ex); CLASS/Oral mucus membrane disorder; CLASS/Mast cell involvement/disorder (ex); CLASS/Spleen disorder (ex)
Pathophysiology: Pathophysiology/Local excess mast cell growth factor; Pathophysiology/Bone marrow infiltration; Pathophysiology/Dysregulated mast cell mediators; Pathophysiology/Point mutation c-kit ligand catalytic domain; Pathophysiology/Stem cell factor c-kit ligand mutation; Pathophysiology/Extreme output gastric acid; Pathophysiology/Fat Malabsorption; Pathophysiology/Fat soluble Vitamin Malabsorption; Pathophysiology/Bronchospasm; Pathophysiology/Osteoporosis Secondary; Pathophysiology/CTSA (Cathepsin A) Gene Mutation; Pathophysiology/D816V c-Kit Mutation; Pathophysiology/Histamine cellular release; Pathophysiology/Mast cell degranulation/activation; Pathophysiology/Mutation Codon 816 c-kit gene
Process: PROCESS/Bimodal age distribution/incidence; PROCESS/Constitutional/essential disorder (ex); PROCESS/Idiopathic/unclassified/unknown (category); PROCESS/Neoplastic (category); PROCESS/Pre-Leukemic condition (ex); PROCESS/Pre-Malignant condition (ex); PROCESS/Reference organ/system (category); PROCESS/Blood dyscrasia/leukemic process (ex); PROCESS/Leukemia process (ex).; PROCESS/Somatic mutation/not hereditary

Synonyms
Synonym: Synonym/Mast cell disease; Synonym/Paucicelluar mastocytosis (TMEP var); Synonym/Telangiectasia macularis eruptiva perstans (var); Synonym/TMEP variant mastocytosis

Treatment
Drug Therapy - Contraindication: RX/Epinephrine (Adrenalin)
Drug Therapy - Indication: RX/Anticholinergics; RX/Anti-H2 receptor medication; RX/Antihistamine medication; RX/Chlorpheniramine (Chlotrimeton); RX/Corticosteroid (Cortisone); RX/Cromolyn sodium/inhaler; RX/Diphenhydramine (Benadryl); RX/Epinephrine (Adrenalin); RX/GM-CSF(Granulocyte-macrophage colony stimulating); RX/Imatinib (Gleevec/Glivec); RX/No effective/definitive treatment yet available; RX/Omeprazole (Prilosec); RX/Oral Cromolyn (cromoglycate); SX/Splenectomy
Surgical Procedures or Treatments: SX/Biopsy
Other Treatments: TX/Diet restriction treatment.; TX/Supportive/Symptomatic treatment

Clinical Manifestations
Signs & Symptoms: Dysphagia Liquids; Dysphagia Progressive; Dysphagia Swallowing Difficulties; Weight loss in Children; Tongue fasciculations; Tongue muscle atrophy; Calf enlargement/bilateral; Calf Pain; Flabby muscles; Head Lag Infant Sign; Hypertrophy leg muscles; Hypotonia; Muscle Atrophy; 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; Mental Deficiency Child; Poor head control/infant; Unable to walk; Waddling Trendelenberg Gait; Weak lower extremities; Weakness/Diffuse motor loss; Dyspnea; Hypoventilation Signs; Respiratory excursions decreased; Shallow breathing; Difficulty learning/school/workplace; Decreased ankle range of motion; Limp; Lumbar lordosis/excess; Delayed speech development/impediment; Difficulty Talking; 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: Males sicker than females/characteristic
Clinical Presentation & Variations: Presentation/Recurrent respiratory infections; Presentation/Congestive heart failure Child
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

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Family History: Family history/Muscle disease/Muscular dystrophy
Sex & Age Groups: Population/Adolescent; Population/Adult/all; Population/Boy patient; Population/Child; Population/Child-Infant Only; Population/Children/all; Population/Male; Population/Toddler; Population/Twenties-Adult/male

Laboratory Tests
Abnormal Lab Findings (Non Measured): Chorionic Villous Sampling Abnormalities; DNATest specific/genetics laboratory/abnormality (Lab)
Abnormal Lab Findings: Aldolase, serum (Lab); CPK/CK/Creatine kinase/Creatine phosphokinase (Lab)

Diagnostic Test Results
Pathology: BX/Muscle Biopsy Abnormal; BX/Muscle biopsy/Increased interstitial tissue; BX/Muscle biopsy/Ribosome count low; BX/Muscle/Non-uniform fiber size
Electrodiagnosis: EMG/Abnormal findings; EMG/Muscular Dystrophic signs
EKG (ECG): EKG/ST Depression Flat T waves V1-V3; EKG/Pseudoinfarction pattern/Q Waves/atypical (ECG); EKG/Q Waves inferior leads (ECG); EKG/R Wave V1 greater than S Wave (ECG); EKG/Abnormal in children; EKG/Changes/abnormalities (ECG)
X-RAY: Xray/Chest abnormal; Xray/Atelectasis/Chest; Xray/Chest/Lung fields/Abnormal

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: Myocarditis; Myocarditis, acute; Polymyositis
Associated Disease & Complications - Causes: Acute respiratory failure/Respiratory arrest; Ankle contracture; Atelectasis, pulmonary; Becker's muscular dystrophy/Pseudohypertrophic; Cardiac arrhythmias; Cardiomyopathy; Cardiomyopathy, secondary; Cognitive/learning disability; Congestive heart failure; Duchenne muscular dystrophy/Pseudohypertrophic; Dyslexia; Hypoventilation, alveolar; Joint contractures; Kyphoscoliosis; Mental retardation; Mitral valve prolapse syndrome; Muscular dystrophy; Obstructive sleep apnea/Children; Paraparesis; Pneumonia; Pneumonia, aspiration; Pneumonia, bacterial; Pneumonia/Bronchopneumonia; Respiratory muscle weakness; Rhabdomyolysis; Tendon contracture, Achilles; Heart Failure in a Child

Disease Mechanism & Classification
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/Lung Hypoventilation; Pathophysiology/Skeletal defomities/acquired; Pathophysiology/Maternal Chromosome mutation
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)

Synonyms
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

Treatment
Drug Therapy: RX/Prednisone (Deltasone)

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