Disease Comparison Results (show differences mode) for Bartter's syndrome and Glanzmann's thrombasthenia

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Glanzmann's thrombasthenia

Found: 66 | Differences: 54

Bartter's syndrome

Found: 153 | Differences: 141

Bartter's syndrome and Glanzmann's thrombasthenia sharing 12 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Bleeding/excessive from mild trauma
Bruising/Ecchymosis
Excessive/easy bruising tendency
Bleeding gums
Bleeding/prolonged dental surgery
Blood in mouth/gums/throat
Epistaxis Children
Epistaxis, severe/persistent
Disease Progression
Course/Improves with time/growth/development
Course/Prolonged/persistent/Not progressive
Course/Subclinical presentation possible
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Bleeding time prolonged/platelet count normal (Lab)
Clot retraction absent (Lab)
Clot retraction formation/abnormal (Lab)
PFA100 (Platelet Function Assay/?) abnormal
Platelet aggregation failure/Ristocetin clumping normal (Lab)
Platelet aggregation/high ADP abnormal (Lab)
Platelet clumping failure on finger stick (Lab)
Platelet collagen aggregation/abnormality (Lab)
Abnormal Lab Findings - Decreased
Factor IX/PTC (Lab)
Platelet count (Lab)
Abnormal Lab Findings - Increased
Bleeding time, Duke (Lab)
Platelet Closure Time
Prothrombin consumption (Lab)
Thromboplastin generation time (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Aspirin platelet defect
Bernard-Soulier syndrome
Hemophilia
Associated Disease & Complications - Causes
Bleeding complications/Surgery
Bleeding diathesis/hemorrhagic diathesis
Bleeding Tendency
Epistaxis/nosebleed
Glanzmann's thrombasthenia
Menorrhagia
Platelet manifestation/defect
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
CLASS/Platelet disorder (ex)
Pathophysiology
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Glycoprotein complex iib/iiia deficiency/platelet
Pathophysiology/GP iib-iiia complex/platelet deficiency
Pathophysiology/Platelet fibrinogen receptor absence
Pathophysiology/Platelet fibrinogen receptor def/Var
Pathophysiology/Platelet glycoprotein (GP 2b/GP 3a) lack
Process
PROCESS/Hereditary platelet disorders (ex)
Synonyms
Synonym
Synonym/Diacyclothrombopathia iib-iiia
Synonym/Glanzmann disease
Synonym/Glanzmann thrombasthenia/type A
Synonym/Glanzmann-Naegeli syndrome
Synonym/GTA
Synonym/Thrombasthenia
Treatment
Drug Therapy
SX/Stem cell transplant/allogenic
SX/Stem-cell transplant
Clinical Manifestations
Signs & Symptoms
Adolescent
Excess Thirst in Children
Stunted growth
Excessive thirst/polydipsia
Poor weight gain/child
Weight loss in Children
Carpopedal spasms
Chvostek's sign
Cramping in Extremities
Episodic muscle weakness
Muscle cramps/spasms
Muscle twitches
Muscle weakness
Proximal muscle weakness
Trousseau's tourniquet sign positive
Twitchy/muscle spasms
Weak/Weak as a kitten (symptom)
Fatigability
Mental Deficiency Child
Spasms in Both Legs
Weakness/Diffuse motor loss
Bed wetting
Diuresis/Large urine volumes
Nocturia
Polyuria
Polyuria and polydipsia
Apparently well Silent disorder possible
Enervated/extreme acute fatigue
Episodic symptoms/events
Fatigue
Fatigue Tiredness Exhaustion
Growth/development delay
Short stature
Short stature Child
Thirst Increased
Water drinking increased
Weakness
Weakness non-neuromuscular/systemic
Weight Loss
Eyelid Fasciculations
Clinical Presentation & Variations
Presentation/Profound Hypokalemia Kids Alkalosis Weak
Presentation/Sensitive to Diuretics Thiazide (Low K)
Demographics & Risk Factors
Population Group
Woman
Family History
Family history/Parental consanguinity
Sex & Age Groups
Population/Adolescent
Population/Child-Infant Only
Population/Female
Population/Old child
Population/Woman patient
Laboratory Tests
Abnormal Lab Findings (Non Measured)
URINE Isosthenuria/mid-range SPGR
Hypercalciuria with normal serum calcium
Hypercalciuria/Normocalcemia pattern
URINE Specific gravity fixed/1.010
Abnormal Lab Findings - Decreased
Chloride serum (Lab)
Magnesium (Lab)
Potassium, serum (Lab)
URINE Specific gravity
Abnormal Lab Findings - Increased
Aldosterone, serum (Lab)
Angiotensin II serum levels (Lab)
Bicarbonate, serum (Lab)
Carbon Dioxide Total Content/CO2
pH, arterial blood (Lab)
Plasma renin Activity/PRA (Lab)
Renin, serum (Lab)
URINE Aldosterone
URINE Calcium
URINE Chloride
URINE Potassium
URINE Prostaglandins
URINE Sodium
Diagnostic Test Results
Pathology
PATH/Adrenocortical hypertrophy
BX/Renal Juxtaglomerular hyperplasia
BX/Renal Renal medulla/interstitial hyperplasia
Electrodiagnosis
EEG/Abnormality
EKG (ECG)
EKG/S-T depression (ECG)
EKG/Prominent U Waves (ECG)
X-RAY
Xray/Bilateral large kidneys/KUB
X-RAY With contrast
IVP/Bilateral large kidneys
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Diabetes insipidus
Hypokalemic periodic paralysis
Nephrogenic diabetes insipidus
Primary hyperaldosteronism
Associated Disease & Complications - Causes
Acid/Base derangement
Alkalosis
Bartter's syndrome
Eneuresis Bed Wetting
Growth retardation/failure
Hyperaldosteronism, secondary
Hypercalciuria
Hypercalcuria
Hypochloremic alkalosis
Hypochloremic metabolic alkalosis
Hypokalemia
Hypokalemic alkalosis
Hypokalemic nephropathy
Hypomagnesemia
Isosthenuria syndrome
Magnesium deficiency
Mental retardation
Metabolic alkalosis
Nephrocalcinosis
Pseudotumor cerebri
Disease Mechanism & Classification
Class
CLASS/Renal tubule defect/manifestation (ex)
CLASS/Renal/kidney involvement/disorder (ex)
CLASS/Urologic (category)
Pathophysiology
Pathophysiology/Gene locus 15q15-q21.1
Pathophysiology/Gene locus 1p36
Pathophysiology/Gene locus Chromosome 1
Pathophysiology/Gene locus Chromosome 15
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Sporadic/hereditary/process
Pathophysiology/Aldosterone excess status
Pathophysiology/Autonomous aldosteronism/dysregulated
Pathophysiology/Erythroepetin autonomous product def
Pathophysiology/Angiotensin II recept absent/congen
Pathophysiology/Hereditary disease renal effect
Pathophysiology/Loop of Henle disorder
Pathophysiology/Renal concentration capacity defect
Pathophysiology/Renal PGE2/Prostagladin E2 excess
Pathophysiology/Renal potassium wastage
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Alkalosis Chloride Resistant
Process
PROCESS/Biochemical (category)
PROCESS/Congenital/developmental (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditary/Non hereditory sets
PROCESS/Vegetative-Autonomic/Endocrine (category)
Synonyms
Synonym
Synonym/Aldosteronism without hypertension syndrome
Synonym/Hyperaldosteronism with normal blood pressure
Synonym/Hyperaldosteronism/hypokalemic alkalosis
Synonym/Hypokalemic alkalosis with hypercalcuria syndrome
Synonym/Juxtaglomerular hyperplasia/aldosteronism
Synonym/Schwartz-Bartter syndrome
Treatment
Drug Therapy
RX/Amiloride (Midamor)
RX/Ibuprofen (Motrin)
RX/Indomethacin (Indocin)
RX/Potassium
RX/Spironolactone (Aldactone)
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