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- Disease Information
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Disease Processes ▼
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Major Organs-Systems ▼
- Systemic
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- Nervous & Sensory System (Neurology)
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Disease Information for Nephrotic syndrome, congenital
- Clinical Manifestations
- Signs & Symptoms
- Edema Children
- Bilateral ankle swelling
- Bilateral leg edema/swelling
- High blood pressure child
- High blood pressure/sign
- Mobile edema/shifts overnight
- Yellow skin discoloration
- Weight gain in Children
- Edema of Lower Extremities
- Nocturia in Children
- Neonatal edema/anasarca
- Weight gain
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Population Group
- Child
- Infant
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population/Infant
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Renal function abnormalities (Lab)
- URINE Protein Electrophoresis (UPE) abnormal
- Abnormal Lab Findings - Decreased
- Transferrin (Lab)
- Tri-iodothyronine/T3 as Resin Uptake (Lab)
- Abnormal Lab Findings - Increased
- Carotene/Vitamin A level (Lab)
- Plasma Retinol
- Plasma Retinol Binding Protein
- URINE Protein (Albumin)
- Diagnostic Test Results
- X-RAY
- Xray/Peritoneal fluid/child/ABD
- Xray/Delayed bone age/slow epiphysis closures
- Xray/Bilateral large kidneys/KUB
- Ultrasound
- Ultrasound/Renal/Kidneys enlarged/symmetrical
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Acute anuria/renal failure
- Ascites
- Ascites in Children
- Azotemia in Children
- Azotemia/Acute
- Carotenemia
- Edema
- Hypertension in a child
- Hypoalbuminemia Hypoproteinemia
- Nephrosis/primary renal disease
- Nephrosis/secondary disease
- Peritoneal Effusion
- Proteinuria
- Renal Failure Chronic
- Proteinuria in Children
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Renal/kidney involvement/disorder (ex)
- CLASS/Urologic (category)
- Pathophysiology
- Pathophysiology/Gene ACTN4 locus 3q
- Pathophysiology/Gene locus 1q25-q31
- Pathophysiology/Gene locus 3q22
- Pathophysiology/Gene locus Chromosome 1
- Pathophysiology/Gene locus chromosome 3
- Pathophysiology/Gene Locus chromosome 3q
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Basement membrane/glomerulus
- Pathophysiology/Intrinsic Parenchymal Renal Failure
- Process
- PROCESS/Congenital/developmental (category)
- PROCESS/Congenital renal disorder (ex)
- PROCESS/Glomerular lesions/disorder (ex)
- Synonyms
- Synonym
- Congenital nephrotic syndr, Congenital Nephrotic Syndrome, Congenital nephrotic syndrome (disorder), Familial nephrotic syndrome, Synonym/Finnish type/congenital nephrotic syndrome
- Treatment
- Surgical Procedures or Treatments
- SX/Biopsy
- Definition
- Be the first to add a definition for Nephrotic syndrome, congenital
- External Links Related to Nephrotic syndrome, congenital
- 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)