Disease Comparison Results (show all mode) for Hemophilia and Myopathy, Myotubular/Centronuclear

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Myopathy, Myotubular/Centronuclear

Found: 65 | Differences: 60

Hemophilia

Found: 163 | Differences: 158

Hemophilia and Myopathy, Myotubular/Centronuclear sharing 5 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Hyperextensable Joints Infant
Constipation Children
Tongue Protrudes Infant
Calf enlargement/bilateral
Delay Sitting Unsupported Infant
Hypotonia
Mouth Hangs Open Infant
Muscle weakness
Muscles Soft/Doughy Infant
Proximal muscle weakness
Rolling Over Delay Infant
Babkin infant sign/Abnormal
Delayed walking milestone/child
Development Motor Skills (Milestones) Delayed
Facial muscle weakness/myopathy
Galant Infant reflex/Abnormal
Head Neck Floppy Infant Hypotonia Sign
Hyporeflexia/DTRs decreased
Infant Head Support Delay
Moro reflex Poor/Absent Infant
Palmar Grasp infant Reflex Abnormal
Primitive infant reflexes/Abnormal
Rooting infant sign/Abnormal
Swimming infant reflex/Abnormal
Tonic Neck Infant reflex/Abnormal
Shallow Breathing Infant
Snoring
Weakness
Double Image Vision Confirmed
Ptosis (blepharoptosis)
Demographics & Risk Factors
Population Group
Infant
Family History
Family history/Muscle disease/Muscular dystrophy
Sex & Age Groups
Population/Infant
Population/Infant male
Population/Male
Diagnostic Test Results
Pathology
BX/Muscle biopsy/centralization of nuclei
Electrodiagnosis
EMG/Abnormal findings
EMG/Myotonic muscle activity
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Eaton-Lambert syndrome
Muscular dystrophy
Polymyositis
Respiratory muscle weakness
Associated Disease & Complications - Causes
Acute respiratory failure/Respiratory arrest
Apnea
Metabolic Myopathy
Myopathy
Neonatal Hypotonia/Floppy Baby Syndrome
Ophthalmoplegia
Ophthalmoplegia/progressive/ext/chronic
Respiratory neonatal distress syndrome
Disease Mechanism & Classification
Class
CLASS/Muscle disorder (ex)
CLASS/Striated muscle disorder (ex)
Pathophysiology
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Disease with many subtypes (ex)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
Clinical Manifestations
Signs & Symptoms
Bleeding from venipuncture sites/needle stick
Bleeding/excessive from mild trauma
Bruising/Ecchymosis
Purpura
Excessive/easy bruising tendency
Bruises/abdomen
Rectal bleeding, gross red
Rectal Blood/Bleeding
Bleeding from Mouth in Elderly
Bleeding from mouth/oral blood
Bleeding gums
Bleeding/prolonged dental surgery
Blood in mouth/gums/throat
Hip Inner Thigh Pain
Vaginal Bleeding
Vaginal bleeding/child
Hemoptysis
Arthralgias Polyarthralgias
Asymmetric hand/feet arthritis
Bilateral knee pains
Discolored Bruised Joint
Discolored Bruised Knee
Enlarged/deformed joints
Hip Pain
Hip Pain In a Child
Hot Joint
Intermittant arthritis syndrome
Joint deformities
Joint effusion
Joint Pains
Joint pains Arthralgias in Children
Joint Swelling
Joint/limit range of motion
Knee manifestation/involvement/secondary
Knee Pain
Large joint involvement/manifestation
Monoarticular Arthritis in Children
Monoarticular Arthritis/One joint acute
Single Joint Pain
Skeletal problems/symptoms/signs
Warm Joint
Epistaxis Children
Epistaxis, severe/persistent
Asymmetric body/build
Episodic symptoms/events
Conjunctival/scleral hemorrhage
Typical Clinical Presentation
Females sicker than males/characteristic
Clinical Presentation & Variations
Presentation/Aggressive Osteoarthritis
Presentation/Single Joint Arthritis
Presentation/Painless Gross hematuria
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Recent Event
Recent/Fall
Recent/MVA
Recent/Trauma
Established Disease Population
Patient/Hemophilia
Population Group
Child
Man
Population/Pediatrics population
Young Adult
Family History
Family history/Bleeding disorders
Family history/Blood disease
Sex & Age Groups
Population/Adult/all
Population/Boy patient
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant male
Population/Male
Population/Man patient
Population/Young adult
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Chorionic Villous Sampling Abnormalities
Chromosomal abnormality (Lab)
Clotting factor assay/abnormal (Lab)
Coagulation/Clotting factors decreased (Lab)
DNATest specific/genetics laboratory/abnormality (Lab)
PTT increased normal PT (Lab)
URINE Dipstick /Blood abnormal
Abnormal Lab Findings - Decreased
Factor 8 (Lab)
Transferrin saturation (Lab)
Abnormal Lab Findings - Increased
Clotting time/Activated clotting time test (Lab)
Hepatitis B surface antigen positive (Lab)
Platelet count (Lab)
PTT/Partial Thromboplastin Time/Activated PTT (Lab)
Recalcification time (Lab)
Thromboplastin generation time (Lab)
TIBC/Total Iron Binding capacity (Lab)
URINE Red blood cells
Diagnostic Test Results
Other Tests & Procedures
Amniocentesis/Abnormality
ThromboElastoGram Abnormal (TEG)
Angiography
Arthrogram/knee many filling defects
Associated Diseases & Rule outs
Associated Disease & Complications
Abdominal wall/muscle hematoma
Arthritis
Bleeding complications/Surgery
Bleeding diathesis/hemorrhagic diathesis
Bleeding Tendency
Cerebral hemorrhage
Chronic hepatitis/Active
Circulating anticoagulants disorder
Circulating coagulation inhibitor status
Epidural hematoma
Epistaxis/nosebleed
Gastrointestinal bleeding
Hemarthrosis
Hematomyelia
Hemophilia
Hemophilic arthritis
Hemothorax
Hepatitis, viral
Hydronephrosis
Internal bleeding/trauma
Intestinal/bowel obstruction
Intracerebral hematoma
Iron deficiency anemia
Jacksonian/posttraumatic epilepsy
Muscle Hematoma
Neck space/Hemorrhage/hematoma
Osteoarthritis, degenerative
Peptic ulcer hemorrhage
Periostitis
Peripheral neuropathy
Polyneuritis
Pseudogout (CPPD) arthritis
Rectus Abdominus Hematoma
Retroperitoneal hemorrhage
Small bowel obstruction
Subarachnoid hemorrhage
Thrombocytosis
Lower GI Bleeding/Infant
Upper GI Bleeding in children
Chronic Hepatitis
Polyneuropathy
Monoarthritis Acute
Hematuria
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene locus Chromosome Xq
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xq28
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Heterozygous/recessive silent/clinically
Pathophysiology/Maternal inheritance
Pathophysiology/Single gene locus indentified
Process
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
PROCESS/Coagulation derangement/disorder (ex)
PROCESS/Hereditary hemorrhagic/coagulation disorder (ex)
Synonyms
Synonym
Synonym/AHG deficiency
Synonym/Factor VIII deficiency
Synonym/Hemophilia A
Treatment
Drug Therapy - Contraindication
RX/Anticoagulants
RX/Warfarin (Coumadin)
Drug Therapy - Indication
RX/Aminocaproic acid (Amicar)
RX/Cryoprecipitate
RX/Desmopressin (DDAVP)
RX/Factor VIII IV Administration
Other Treatments
TX/Cultured Fibroblasts Infusion
TX/Genetic counselling
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