Disease Comparison Results (show differences mode) for Cirrhosis/childhood Indian type and Familial Cold Autoinflammatory syndrome/FCAS (1q44).

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Cirrhosis/childhood Indian type

Found: 146 | Differences: 143

Cirrhosis/childhood Indian type and Familial Cold Autoinflammatory syndrome/FCAS (1q44). sharing 3 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Cold urticaria
Ice Cube test/Urticaria Abnormal
Rash
Excess Thirst in Children
Arthritis Children
Cold intolerance
Cyclic Periodic Recurrent Fevers
Periodic fever
Bloodshot eyes/Conjunctival injection
Eye Pains, Bilateral
Red Eyes Bilateral
Scleral Injection
Disease Progression
Course/Periodic Episodic
Onset childhood/young adult/twenties
Laboratory Tests
Microbiology & Serology Findings
Stool Microscopic polys present
Abnormal Lab Findings (Non Measured)
Acute phase reactants increased (Lab)
Abnormal Lab Findings
WBC
Amyloid A serum (Lab)
C-reactive protein (Lab)
Interleukin 1 (IL-1) levels (Lab)
Interleukin-6 IL-6 Serum (Lab)
Serum Amyloid A (SSA)
WBC/White Blood Cell Count/Leukocytes (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications
Amyloidosis, renal
Amyloidosis, systemic
Arthritis
Conjunctivitis
Deafness
Deafness, sensorineural
Familial Cold Autoinflammatory syndrome/FCAS (1q44).
Polyarthritis in Children
Polyarthritis syndrome/Multiple joints/weeks
Urticaria, cold/immersion
Urticaria/hives
PolyArthritis
Disease Mechanism & Classification
Pathophysiology
Pathophysiology/Autoinflammatory (non-immune)
Pathophysiology/Gene locus 1q44
Pathophysiology/Gene locus Chromosome 1
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Auto-Inflammatory Disorder
Pathophysiology/Excess Interleukin I (IL-1) produced
Pathophysiology/CIAS1 Gene mutation
Pathophysiology/CIAS1/NLRP-3 Gene Mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/INCIDENCE/Extremely rare disease
Synonyms
Synonym
Synonym/FCAS
Synonym/Muckles Wells Syndrome/FCAS (1q44)
Treatment
Drug Therapy
RX/Canakinumab (Llaris)
RX/Rilonacept IL-1 Blocker (Arcalyst)
Clinical Manifestations
Signs & Symptoms
Edema Children
Bilateral ankle swelling
Bilateral leg edema/swelling
Clubbing
Clubbing of fingers/toes
Bruising/Ecchymosis
Prominent venous plexus/cutaneous
Spider nevi/angiomata/Abdominal sign
Telangiectasias in Children
Yellow skin discoloration
Excessive/easy bruising tendency
Anorexia Decreased appetite
Caput medusa/abdomen
Signs of ascites
Chest/truncal venous distension
Fever with Jaundice
Jaundice of newborn
Jaundice/Yellow skin and eyes
Liver firm/edge indurated
Liver palms/erythema
Palpable Liver/Hepatomegaly
Yellow eyeballs/Scleral icterus
Edema of Lower Extremities
Palmar Erythema/Redness
Epistaxis Children
Dark urine
Chronically ill patient/signs
Debilitated
Fatigue Tiredness in Children
Fever
Fever Febrile Possible
Flu-Like Syndrome
High body temperature
Short stature Child
Typical Clinical Presentation
Presentation/Painless/jaundice
Clinical Presentation & Variations
Presentation/Cirrhosis Non-Alcoholic
Disease Progression
Course/Chronic disorder
Course/Lethal
Course/Prognosis bad/usually
Course/Progressive
Course/Relentless
Course/Severe illness
Course/Subacute
Onset ages 2 to 3 yrs
Onset/Childhood
Demographics & Risk Factors
Exposure Factors
Exposure/Epidemiologic specific setting/exposure
Exposure/Use/Copper cooking/storage vessels
Travel, Geographic & Climate Related Factors
Residence/travel/Africa
Residence/travel/Central America
Residence/travel/Middle East
Residence/travel/Rural area
Ethnic or Racial Factors
African black population
Asian Indian population
Egyptian population
Middle Eastern Population
Population Group
Child
Population/Immigrant population
Population/Pediatrics population
Family History
Family history/Liver disease
Family history/Liver disease Children
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
ASCITIC Transudates (Ex)
Acute inflammatory markers elevated (Lab)
Fasting hypoglycemia (Lab)
Hepatic Enzymes Abnormal (Lab)
Immunelectrophoresis polyclonal globulin (Lab)
Liver Functions Abnormal (Lab)
Protein electrophoresis/Beta-Gamma Peaks Serum)
SAAG Serum Ascites-albumin gradient/high (Lab)
Transaminase elevation (Lab)
Abnormal Lab Findings - Decreased
Albumin, serum (Lab)
ASCITIC Protein
Abnormal Lab Findings - Increased
Alkaline phosphatase, liver isoenzyme/serum (Lab)
Alkaline phosphatase, serum (Lab)
ALT (SGPT) (Alanine transferase) (Lab)
Ammonia blood (Lab)
Aspartamine aminotransferase (SGOT, AST) (Lab)
AST (SGOT) (aspartamine transferase) (Lab)
Bilirubin, serum (Lab)
Copper, serum (Lab)
Estradiol Serum (Lab)
Gamma globulin (Lab)
Globulin, serum (Lab)
IGG/Immunoglobulin G (Lab)
URINE Estrogens
URINE/Estradiol (Lab)
URINE/Estratriol (Lab)
Diagnostic Test Results
Other Tests & Procedures
Gastroscopy/Esophageal varices
Paracentesis/Abnormality
Pathology
BX/Liver biopsy/Abnormal
BX/Liver biopsy/Copper deposit/tissue
BX/Liver biopsy/Mallory bodies
CT Scan
CT Scan/Ascites signs
CT Scan/Liver abnormality
CT Scan/Liver Caudate/Right lobe size ratio >.65
CT Scan/Liver Portasystemic venous collaterals
CT Scan/Liver Right lobe/atrophy/Left/caudate enlarged
CT Scan/Spleen enlarged
X-RAY
Xray/Peritoneal fluid/child/ABD
X-RAY With contrast
UGI/Esophageal varices
Ultrasound
Ultrasound/Abdomen/Liver small
Ultrasound/Spleen enlarged
Associated Diseases & Rule outs
Associated Disease & Complications
Ascites
Ascites in Children
Bilirubinemia
Bleeding esophageal varices
Cirrhosis
Cirrhosis in childhood
Cirrhosis, childhood/Indian type
Edema
Epistaxis/nosebleed
Esophageal varices
Hepatic failure
Hyperammonemia
Hyperglobulinemia
Hypoalbuminemia Hypoproteinemia
Peritoneal Effusion
Portal hypertension
Telangiectasia
Upper GI Bleeding in children
Disease Mechanism & Classification
Class
CLASS/Hepatic architecture disorder (ex)
CLASS/Liver involvement/disorder (ex)
Pathophysiology
Pathophysiology/Copper accumulation/tissues
Pathophysiology/Bleeding from Portal Veins
Pathophysiology/Hepatic manifestations/involvement
Process
PROCESS/Copper/metabolism disorders (ex)
PROCESS/Hereditary/Genetic predisposition (ex)
PROCESS/INCIDENCE/Regional specific
PROCESS/Poisoned organ/system (category)
Treatment
Drug Therapy
RX/Penicillamine (Cupramine)
RX/Trientine (Syprine/Cuprid)
Surgical Procedures or Treatments
SX/Biopsy
SX/Liver biopsy
SX/Liver transplant
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