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Article

Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.

Archives of Iranian medicine - 1 Apr 2023

Zare Ashrafi Farzane, Akhtarkhavari Tara, Fattahi Zohreh, Asadnezhad Maryam, Beheshtian Maryam, Arzhangi Sanaz, Najmabadi Hossein, Kahrizi Kimia

Abstract excerpt

BACKGROUND: Intellectual disability (ID) is a genetically heterogeneous condition, and so far, 1679 human genes have been identified for this phenotype. Countries with a high rate of parental consanguinity, such as Iran, provide an excellent opportunity to identify the remaining novel ID genes, especially those with an autosomal recessive (AR) mode of inheritance. This study aimed to investigate the most...

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Identifiers

PMID: 38301078
DOI: 10.34172/aim.2023.29
PMCID: PMC10685746

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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