<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>77(1)</volume><submitter>Patel V</submitter><pubmed_abstract>The chromosomal characterization of nasopharyngeal angiofibroma (NPF) of Indian origin seems important as it is consistently absent in literature. Routine karyotyping (G-banding) and fluorescence in situ hybridization (FISH) analysis was undertaken using CMYC, TP53 CEPX/Y probes in 9 cases of NPF wherein chromosomal characteristics were correlated with clinical parameters. Karyotype profile of venous sample from every case was normal. Following FISH analysis, 5 (55%) cases showed deleted CMYC allele while 4 (44%) showed deleted TP53. In addition, loss of Y centromere was evident in 1 case. Despite definite trends, no significant correlation with clinical parameters and FISH expression/ G-banding karyotyping could be appreciated. The peripheral blood karyotype cannot predict any significant</pubmed_abstract><journal>Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India</journal><pagination>284-290</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11890675</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Nasopharyngeal Angiofibroma: Karyotyping Profile and Florescent In-Situ Hybridization Analysis with C-Myelocytomatosis, Tumor Suppressor p53 and CEP-X/Y Probes.</pubmed_title><pmcid>PMC11890675</pmcid><pubmed_authors>Singh MK</pubmed_authors><pubmed_authors>Mishra A</pubmed_authors><pubmed_authors>Patel V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nasopharyngeal Angiofibroma: Karyotyping Profile and Florescent In-Situ Hybridization Analysis with C-Myelocytomatosis, Tumor Suppressor p53 and CEP-X/Y Probes.</name><description>The chromosomal characterization of nasopharyngeal angiofibroma (NPF) of Indian origin seems important as it is consistently absent in literature. Routine karyotyping (G-banding) and fluorescence in situ hybridization (FISH) analysis was undertaken using CMYC, TP53 CEPX/Y probes in 9 cases of NPF wherein chromosomal characteristics were correlated with clinical parameters. Karyotype profile of venous sample from every case was normal. Following FISH analysis, 5 (55%) cases showed deleted CMYC allele while 4 (44%) showed deleted TP53. In addition, loss of Y centromere was evident in 1 case. Despite definite trends, no significant correlation with clinical parameters and FISH expression/ G-banding karyotyping could be appreciated. The peripheral blood karyotype cannot predict any significant</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-05-27T08:00:45.733Z</modification><creation>2026-05-27T03:12:22.322Z</creation></dates><accession>S-EPMC11890675</accession><cross_references><pubmed>40066402</pubmed><doi>10.1007/s12070-024-05171-z</doi></cross_references></HashMap>