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
Marina Dr Marina Aksenova Poster Presenter
A Case of Smoldering Atypical HUS Superimposed on Familial FSGS
WCN24-AB-2091, Poster Board= MON-182
Elias Bassil Poster Presenter
POTTER SYNDROME IN BRAZIL: A CROSS-SECTIONAL ANALYSIS, 2011-2021
WCN24-AB-1346, Poster Board= 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
INTERMITTENT RHABDOMYOLYSIS IN A PATIENT WITH ACYL-COA DEFICIENCY VERY LONG CHAIN DEHYDROGENASE.
WCN24-AB-376, Poster Board= MON-185
PHENOTYPES OF PATIENTS WITH ATYPICAL HEMOLYTIC UREMIC SYNDROME
WCN24-AB-882, Poster Board= 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
Paola Krall Poster Presenter
AN UNUSUAL CAUSE OF NEUROGENIC BLADDER IN A CHILD
WCN24-AB-1142, Poster Board= 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
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
Carolina Rojas Salinas Poster Presenter
Prevalence of Germline Pathogenic Variants in Filipino Patients with Renal Cell Carcinoma
WCN24-AB-249, Poster Board= MON-191
Larraine Vergara-Rejante Poster Presenter
GENETIC ANALYSIS IN DIARRHEA-ASSOCIATED STEC NEGATIVE HEMOLYTIC UREMIC SYNDROME
WCN24-AB-1143, Poster Board= 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
Federico Yandian Poster Presenter
ARSENIC TRIOXIDE ATTENUATES MMP9/IL-17A EXPRESSION IN LUPUS NEPHRITIS
WCN24-AB-659, Poster Board= MON-194
Desmond Yap Poster Presenter