<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Ali Khan Q</submitter><pubmed_abstract>Background Intellectual disability (ID), also termed mental retardation (MR), is a neurodevelopmental disorder characterized by an intelligence quotient (IQ) of 70 or below and a deficit in at least two behaviors associated with adaptive functioning. The condition is further classified into syndromic intellectual disability (S-ID) and non-syndromic intellectual disability (NS-ID). This study highlights the genes associated with NS-ID. Objectives A genetic study was performed on two Pakistani families to know the inheritance patterns, clinical phenotypes, and molecular genetics of affected individuals with NS-ID. Methodology Samples were collected from two families: families A and B. All affected individuals in both families were diagnosed by a neurologist. Written informed consent was take</pubmed_abstract><journal>Cureus</journal><pagination>e34085</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9946902</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Non-syndromic Intellectual Disability: An Experimental In-Depth Exploration of Inheritance Pattern, Phenotypic Presentation, and Genomic Composition.</pubmed_title><pmcid>PMC9946902</pmcid><pubmed_authors>Vattikuti B</pubmed_authors><pubmed_authors>Shahzadi A</pubmed_authors><pubmed_authors>Verma R</pubmed_authors><pubmed_authors>Farkouh M</pubmed_authors><pubmed_authors>Santiago N</pubmed_authors><pubmed_authors>Abdi P</pubmed_authors><pubmed_authors>Farkouh CS</pubmed_authors><pubmed_authors>Shah SD</pubmed_authors><pubmed_authors>Ali Khan Q</pubmed_authors><pubmed_authors>Nunez A</pubmed_authors><pubmed_authors>Anthony M</pubmed_authors><pubmed_authors>Khan AZ</pubmed_authors><pubmed_authors>Zepeda D</pubmed_authors><pubmed_authors>Khan R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Non-syndromic Intellectual Disability: An Experimental In-Depth Exploration of Inheritance Pattern, Phenotypic Presentation, and Genomic Composition.</name><description>Background Intellectual disability (ID), also termed mental retardation (MR), is a neurodevelopmental disorder characterized by an intelligence quotient (IQ) of 70 or below and a deficit in at least two behaviors associated with adaptive functioning. The condition is further classified into syndromic intellectual disability (S-ID) and non-syndromic intellectual disability (NS-ID). This study highlights the genes associated with NS-ID. Objectives A genetic study was performed on two Pakistani families to know the inheritance patterns, clinical phenotypes, and molecular genetics of affected individuals with NS-ID. Methodology Samples were collected from two families: families A and B. All affected individuals in both families were diagnosed by a neurologist. Written informed consent was take</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T09:48:49.806Z</modification><creation>2024-11-05T18:12:21.034Z</creation></dates><accession>S-EPMC9946902</accession><cross_references><pubmed>36843831</pubmed><doi>10.7759/cureus.34085</doi></cross_references></HashMap>