Genetics and Epigenetics (Including Common and Rare Genetic Diseases) 3

15 Apr 2024 5:45 p.m. 6:45 p.m.

MON-181 to MON-194

Sebastián Jaurretche Poster Moderator

Time	Session

5:45 p.m. 6:45 p.m.	DO CHILDREN WITH ALPORT SYNDROME HAVE AN INCREASED RISK OF AORTIC DILATATION? WCN24-AB-2111, Poster Board= MON-181 MON-181 Marina Dr Marina Aksenova Poster Presenter	A Case of Smoldering Atypical HUS Superimposed on Familial FSGS WCN24-AB-2091, Poster Board= MON-182 MON-182 Elias Bassil Poster Presenter	POTTER SYNDROME IN BRAZIL: A CROSS-SECTIONAL ANALYSIS, 2011-2021 WCN24-AB-1346, Poster Board= MON-183 MON-183 Geraldo Bezerra Da Silva Junior Poster Presenter	FAMILIAL GLOBAL AND FOCAL GLOMERULOSCLEROSIS: AUTOSOMAL DOMINANT TUBULOINTERSTITIAL KIDNEY DISEASE (ADTKD) DUE TO C.610C>G MUTATION IN UMOD GENE WCN24-AB-2395, Poster Board= MON-184 MON-184	INTERMITTENT RHABDOMYOLYSIS IN A PATIENT WITH ACYL-COA DEFICIENCY VERY LONG CHAIN DEHYDROGENASE. WCN24-AB-376, Poster Board= MON-185 MON-185	PHENOTYPES OF PATIENTS WITH ATYPICAL HEMOLYTIC UREMIC SYNDROME WCN24-AB-882, Poster Board= MON-186 MON-186 Ekaterina Ivanova Poster Presenter	A complex pediatric case with homozygous IFT140 variants involving renal cysts: a comprehensive analysis to guide diagnosis and patient care WCN24-AB-850, Poster Board= MON-187 MON-187 Paola Krall Poster Presenter	AN UNUSUAL CAUSE OF NEUROGENIC BLADDER IN A CHILD WCN24-AB-1142, Poster Board= MON-188 MON-188 Haruna Mahama Poster Presenter	HISTOPATHOLOGICAL CHARACTERISTICS IN CHILDREN WITH MONOGENIC AND NON-GENETIC STEROID-RESISTANT NEPHROTIC SYNDROME WCN24-AB-1772, Poster Board= MON-189 MON-189 Larisa Prikhodina Poster Presenter	CHARCOT-MARIE-TOOTH SYNDROME AND GENETIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: DE NOVO MUTATION OF THE INF2 GENE WCN24-AB-2383, Poster Board= MON-190 MON-190 Carolina Rojas Salinas Poster Presenter	Prevalence of Germline Pathogenic Variants in Filipino Patients with Renal Cell Carcinoma WCN24-AB-249, Poster Board= MON-191 MON-191 Larraine Vergara-Rejante Poster Presenter	GENETIC ANALYSIS IN DIARRHEA-ASSOCIATED STEC NEGATIVE HEMOLYTIC UREMIC SYNDROME WCN24-AB-1143, Poster Board= MON-192 MON-192 Marina Vivarelli Poster Presenter	Alport Syndrome: genetic variants, phenotypes of kidney disease and association with End Stage Kidney Disease in a Uruguayan Cohort WCN24-AB-864, Poster Board= MON-193 MON-193 Federico Yandian Poster Presenter	ARSENIC TRIOXIDE ATTENUATES MMP9/IL-17A EXPRESSION IN LUPUS NEPHRITIS WCN24-AB-659, Poster Board= MON-194 MON-194 Desmond Yap Poster Presenter