Genetics and Epigenetics (Including Common and Rare Genetic Diseases) 2

8 Feb 2025 5:30 p.m. 6:30 p.m.

Debrabata Mukherjee Moderator

Time	Session

12 a.m. 12 a.m.	FAMILIAL IGA NEPHROPATHY: A PERPLEXING CONUNDRUM IN A FAMILY WCN25-AB-1449, Poster Board= SAT-256	MUTATIONAL SPECTRUM OF CTNS GENE IN INDIAN CHILDREN WITH NEPHROPATHIC CYSTINOSIS WCN25-AB-2709, Poster Board= SAT-257	HIGH YIELD OF GENETIC TESTING IN NEPHROLOGY-A STUDY FROM TERTIARY CARE CENTRE IN SOUTH INDIA WCN25-AB-1520, Poster Board= SAT-258	A RARE COMBINATION OF BARDET-BIEDL AND MECKEL SYNDROME: A CASE REPORT WCN25-AB-1707, Poster Board= SAT-259	RENAL TRANSPLANTATION IN AMYLOIDOSIS DUE TO NOVEL MUTATION OF APOLIPOPROTEIN A- II: FIRST ASIAN CASE REPORT WCN25-AB-2715, Poster Board= SAT-260	NEXT-GENERATION SEQUENCING FOR CYSTIC KIDNEY DISEASE: A MULTI-CENTER CROSS-SECTIONAL STUDY FROM INDIA WCN25-AB-2466, Poster Board= SAT-261	GENETIC VARIATIONS AND OUTCOMES IN CHILDREN WITH RENAL TUBULAR DISORDERS: INSIGHTS FROM INDIAN TUBULOPATHY REGISTRY WCN25-AB-2591, Poster Board= SAT-262	COMPLEMENT GENE MUTATIONS IN PATIENTS WITH CHRONIC KIDNEY DISEASE ON DIALYSIS (CKD-D) OF UNKNOWN ETIOLOGY: OUR EXPERIENCE FROM CENTRAL INDIA WCN25-AB-2706, Poster Board= SAT-263	A CASE STUDY OF HELIX SYNDROME: NOVEL MUTATION ASSOCIATED WITH METABOLIC ALKALOSIS AND HYPOKALEMIA IN PEDIATRICS. WCN25-AB-2756, Poster Board= SAT-264	APOLIPOPROTIEN E IN C3 GLOMERULOPATHAY-A VALIDATION WCN25-AB-3225, Poster Board= SAT-265	KIDNEY TRANSPLANTATION IN PRESENCE OF COMPLEMENT GENE MUTATIONS IN BOTH RECIPIENTS AND THEIR ASYMPTOMATIC KIDNEY DONORS: OUR EXPERIENCE FROM CENTRAL INDIA WCN25-AB-2825, Poster Board= SAT-266	BIZARRE CLINICAL PRESENTATIONS OF DISORDERS OF COMPLEMENT DYSREGULATION – CASE SERIES WCN25-AB-3856, Poster Board= SAT-267	RENAL DENERVATION IN LOIN PAIN HEMATURIA SYNDROME: A FEASIBILITY RANDOMIZED CONTROL TRIAL WCN25-AB-3548, Poster Board= SAT-268	AN INTERESTING CASE REPORT OF MINIMAL CHANGE DISEASE PRESENTING AS NEPHROTIC SYNDROME IN YOUNG FEMALE WITH PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE WCN25-AB-4107, Poster Board= SAT-269	THE FITNESS PARADOX WCN25-AB-4233, Poster Board= SAT-270	CHALLENGES AND DILEMMA WITH RENAL TRANSPLANT IN AUTOSOMAL ALPORT SYNDROME AND ROLE OF NEXT GENERATION SEQUENCING, A CASE REPORT WCN25-AB-4309, Poster Board= SAT-271	EXOME ANALYSIS POINTS APOE4 HAPLOTYPE AS MAJOR RISK TO DEVELOP MESOAMERICAN NEPHROPATHY WCN25-AB-4604, Poster Board= SAT-272	GENOTYPIC-PHENOTYPIC SPECTRUM OF COL4 MUTATION & TRANSPLANT OUTCOME OF ALPORT SYNDROME: A SINGLE CENTRE EXPERIENCE WCN25-AB-2081, Poster Board= SAT-273