- A Family with Autosomal Dominant Alport Syndrome with Phenotypic Variability
10:00 AM - 12:00 PM
A Family with Autosomal Dominant Alport Syndrome with Phenotypic Variability
October 24, 2024 | 10:00 AM - 12:00 PM
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- Resolution of Two Intronic Noncanonical Splicing Variants Located in X-linked Alport COL4A5 Gene
10:00 AM - 12:00 PM
Resolution of Two Intronic Noncanonical Splicing Variants Located in X-linked Alport COL4A5 Gene
October 24, 2024 | 10:00 AM - 12:00 PM
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- Unveiling X-linked Alport Syndrome: Genetic Testing in FSGS
10:00 AM - 12:00 PM
Unveiling X-linked Alport Syndrome: Genetic Testing in FSGS
October 24, 2024 | 10:00 AM - 12:00 PM
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- A Case of Autosomal Dominant Hereditary Nephritis
10:00 AM - 12:00 PM
A Case of Autosomal Dominant Hereditary Nephritis
October 24, 2024 | 10:00 AM - 12:00 PM
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- Unusual Glomerular Abnormalities in a Patient with Combined COL4A5-NPHS1 Variants
10:00 AM - 12:00 PM
Unusual Glomerular Abnormalities in a Patient with Combined COL4A5-NPHS1 Variants
October 24, 2024 | 10:00 AM - 12:00 PM
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- Alport Syndrome in Iceland: Epidemiology and Outcomes
10:00 AM - 12:00 PM
Alport Syndrome in Iceland: Epidemiology and Outcomes
October 24, 2024 | 10:00 AM - 12:00 PM
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- Ocular Coherence Tomography Unveils Alport Syndrome: A Critical Tool in Detecting Collagen IV Nephropathies
10:00 AM - 12:00 PM
Ocular Coherence Tomography Unveils Alport Syndrome: A Critical Tool in Detecting Collagen IV Nephropathies
October 24, 2024 | 10:00 AM - 12:00 PM
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- Variants Involving Podocyte and Extracellular Matrix Proteins in Alport Syndrome: A Case Series
10:00 AM - 12:00 PM
Variants Involving Podocyte and Extracellular Matrix Proteins in Alport Syndrome: A Case Series
October 24, 2024 | 10:00 AM - 12:00 PM
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- Role of Family History and Genetic Testing in Diagnosing Rare Diseases
10:00 AM - 12:00 PM
Role of Family History and Genetic Testing in Diagnosing Rare Diseases
October 24, 2024 | 10:00 AM - 12:00 PM
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- Unwrapping the Enigma: A Rare Case of MYH9 Nephropathy
10:00 AM - 12:00 PM
Unwrapping the Enigma: A Rare Case of MYH9 Nephropathy
October 24, 2024 | 10:00 AM - 12:00 PM
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- A Boy with Steroid-Resistant Nephrotic Syndrome and Cortical Blindness
10:00 AM - 12:00 PM
A Boy with Steroid-Resistant Nephrotic Syndrome and Cortical Blindness
October 24, 2024 | 10:00 AM - 12:00 PM
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- Clinical and Genetic Assessment for the Mechanisms Underlying Phenotypic Diversity in Steroid-Resistant Nephrotic Syndrome Caused by TRPC6 Variants
10:00 AM - 12:00 PM
Clinical and Genetic Assessment for the Mechanisms Underlying Phenotypic Diversity in Steroid-Resistant Nephrotic Syndrome Caused by TRPC6 Variants
October 24, 2024 | 10:00 AM - 12:00 PM
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- Combined Genetics and Ultrastructural Examination in Diagnosis and Treatment Decisions of Focal and Segmental Glomerulosclerosis
10:00 AM - 12:00 PM
Combined Genetics and Ultrastructural Examination in Diagnosis and Treatment Decisions of Focal and Segmental Glomerulosclerosis
October 24, 2024 | 10:00 AM - 12:00 PM
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- May-Hegglin Anomaly-Associated Nephropathy: A Case Series
10:00 AM - 12:00 PM
May-Hegglin Anomaly-Associated Nephropathy: A Case Series
October 24, 2024 | 10:00 AM - 12:00 PM
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- Case Report of a Novel NRIP1 Gene Mutation: Disease Association or Mere Coincidence?
10:00 AM - 12:00 PM
Case Report of a Novel NRIP1 Gene Mutation: Disease Association or Mere Coincidence?
October 24, 2024 | 10:00 AM - 12:00 PM
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- Hiding in Plain Sight: The Diagnostic Challenge of Autosomal Dominant Tubulointerstitial Kidney Disease
10:00 AM - 12:00 PM
Hiding in Plain Sight: The Diagnostic Challenge of Autosomal Dominant Tubulointerstitial Kidney Disease
October 24, 2024 | 10:00 AM - 12:00 PM
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- Chronic Benign Tubular Proteinuria from Compound Heterozygous Mutations in CUBN: A Case Report
10:00 AM - 12:00 PM
Chronic Benign Tubular Proteinuria from Compound Heterozygous Mutations in CUBN: A Case Report
October 24, 2024 | 10:00 AM - 12:00 PM
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- Cases of Patients with E66Q Mutation Manifesting Zebra Bodies in Various Organs
10:00 AM - 12:00 PM
Cases of Patients with E66Q Mutation Manifesting Zebra Bodies in Various Organs
October 24, 2024 | 10:00 AM - 12:00 PM
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- Fishing for Zebras: Catching Fabry Disease with Pretransplant Genetic Testing
10:00 AM - 12:00 PM
Fishing for Zebras: Catching Fabry Disease with Pretransplant Genetic Testing
October 24, 2024 | 10:00 AM - 12:00 PM
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- Fabry Nephropathy: An Important Phenotype of the Mutation p.R356W (c.1066C>T)
10:00 AM - 12:00 PM
Fabry Nephropathy: An Important Phenotype of the Mutation p.R356W (c.1066C>T)
October 24, 2024 | 10:00 AM - 12:00 PM
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- MMP1 Levels in Kidney Tissue May Be Related to Kidney Interstitial Fibrosis in Fabry Disease
10:00 AM - 12:00 PM
MMP1 Levels in Kidney Tissue May Be Related to Kidney Interstitial Fibrosis in Fabry Disease
October 24, 2024 | 10:00 AM - 12:00 PM
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- Influenza B Triggering Atypical Hemolytic Uremic Syndrome (aHUS) in a Patient with Cobalamin C (CblC) Disease Carrier State and a Complement Factor H (CFH) Mutation
10:00 AM - 12:00 PM
Influenza B Triggering Atypical Hemolytic Uremic Syndrome (aHUS) in a Patient with Cobalamin C (CblC) Disease Carrier State and a Complement Factor H (CFH) Mutation
October 24, 2024 | 10:00 AM - 12:00 PM
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- Atypical Hemolytic Uremic Syndrome with Peripheral Gangrene
10:00 AM - 12:00 PM
Atypical Hemolytic Uremic Syndrome with Peripheral Gangrene
October 24, 2024 | 10:00 AM - 12:00 PM
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- A Case of Atypical Hemolytic Uremic Syndrome with a Complement Factor I Mutation Triggered by a Femoral Neck Fracture in an Elderly Japanese Patient
10:00 AM - 12:00 PM
A Case of Atypical Hemolytic Uremic Syndrome with a Complement Factor I Mutation Triggered by a Femoral Neck Fracture in an Elderly Japanese Patient
October 24, 2024 | 10:00 AM - 12:00 PM
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- Sex-Specific Modulation of Renal Dopamine Receptor Expression by DRD2 Single-Nucleotide Polymorphisms (SNPs) and Hormonal Factors
10:00 AM - 12:00 PM
Sex-Specific Modulation of Renal Dopamine Receptor Expression by DRD2 Single-Nucleotide Polymorphisms (SNPs) and Hormonal Factors
October 24, 2024 | 10:00 AM - 12:00 PM
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- Kidney Disease Due to Caudal Regression Syndrome
10:00 AM - 12:00 PM
Kidney Disease Due to Caudal Regression Syndrome
October 24, 2024 | 10:00 AM - 12:00 PM
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- AA Amyloidosis Unveiling Familial Mediterranean Fever in a 65-Year-Old Armenian Man with Arthritis and Immunosuppression History
10:00 AM - 12:00 PM
AA Amyloidosis Unveiling Familial Mediterranean Fever in a 65-Year-Old Armenian Man with Arthritis and Immunosuppression History
October 24, 2024 | 10:00 AM - 12:00 PM
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- A Case of Prolonged Glycosuria Secondary to SLC5A2 Receptor Mutation Affecting theSGLT2
10:00 AM - 12:00 PM
A Case of Prolonged Glycosuria Secondary to SLC5A2 Receptor Mutation Affecting theSGLT2
October 24, 2024 | 10:00 AM - 12:00 PM
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- Acute Kidney Failure: An Atypical Presentation of Gordon Syndrome
10:00 AM - 12:00 PM
Acute Kidney Failure: An Atypical Presentation of Gordon Syndrome
October 24, 2024 | 10:00 AM - 12:00 PM
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- Increased Risk of Kidney Injury and Early Death from Activating Mutations in the Calcium-Sensing Receptor: A Regional Case Series
10:00 AM - 12:00 PM
Increased Risk of Kidney Injury and Early Death from Activating Mutations in the Calcium-Sensing Receptor: A Regional Case Series
October 24, 2024 | 10:00 AM - 12:00 PM
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- OMg! What Links Hypomagnesemia, Kidney Stones, and Arrhythmia
10:00 AM - 12:00 PM
OMg! What Links Hypomagnesemia, Kidney Stones, and Arrhythmia
October 24, 2024 | 10:00 AM - 12:00 PM
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- Ceroid Lipofuscin in Renal Tubular Cells in Hermsky Pudlak Syndrome (HPS): An Unexplored Entity
10:00 AM - 12:00 PM
Ceroid Lipofuscin in Renal Tubular Cells in Hermsky Pudlak Syndrome (HPS): An Unexplored Entity
October 24, 2024 | 10:00 AM - 12:00 PM
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- Deafness and Bilateral Staghorn Kidney Stones in a Young Patient
10:00 AM - 12:00 PM
Deafness and Bilateral Staghorn Kidney Stones in a Young Patient
October 24, 2024 | 10:00 AM - 12:00 PM
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- Triple Threat! A Case of Lowe Syndrome with Triple Genetic Mutations
10:00 AM - 12:00 PM
Triple Threat! A Case of Lowe Syndrome with Triple Genetic Mutations
October 24, 2024 | 10:00 AM - 12:00 PM
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- Unraveling the Mystery: McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure
10:00 AM - 12:00 PM
Unraveling the Mystery: McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure
October 24, 2024 | 10:00 AM - 12:00 PM
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- Nail-Patella Syndrome Presenting with Nephrotic Syndrome during Pregnancy
10:00 AM - 12:00 PM
Nail-Patella Syndrome Presenting with Nephrotic Syndrome during Pregnancy
October 24, 2024 | 10:00 AM - 12:00 PM
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- All in the Genes: Chronic Benign Proteinuria Due to CUBN Mutations
10:00 AM - 12:00 PM
All in the Genes: Chronic Benign Proteinuria Due to CUBN Mutations
October 24, 2024 | 10:00 AM - 12:00 PM
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- Sex Differences in Primary Distal Renal Tubular Acidosis
10:00 AM - 12:00 PM
Sex Differences in Primary Distal Renal Tubular Acidosis
October 24, 2024 | 10:00 AM - 12:00 PM
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- Towne Brocks Syndrome Presenting as ESKD
10:00 AM - 12:00 PM
Towne Brocks Syndrome Presenting as ESKD
October 24, 2024 | 10:00 AM - 12:00 PM
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- Patient Satisfaction and Outcomes following a Session with a Genetic Counselor for Kidney Diseases
10:00 AM - 12:00 PM
Patient Satisfaction and Outcomes following a Session with a Genetic Counselor for Kidney Diseases
October 24, 2024 | 10:00 AM - 12:00 PM
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- Nephrologists' Views and Experience with Genetic Testing: Developing vs. Developed Countries
10:00 AM - 12:00 PM
Nephrologists' Views and Experience with Genetic Testing: Developing vs. Developed Countries
October 24, 2024 | 10:00 AM - 12:00 PM
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