» Articles » PMID: 17952016

'Mental Retardation' or 'intellectual Disability': Time for a Conceptual Change

Overview
Journal Psychopathology
Specialty Psychiatry
Date 2007 Oct 24
PMID 17952016
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The term 'mental retardation' (MR) is outdated and has changed to 'intellectual disability' (ID). Unfortunately, this decision did not follow a nosology approach. The aim of this overview is twofold: (1) to provide a conceptual background and framing on the ID/MR field to other psychiatrists, and (2) to provide a nosology-based perspective to the debate on the name and concept of MR/ID.

Method: This conceptual paper is based on a literature review and on an iterative process of debate within the WPA Section 'Psychiatry of Mental Retardation'.

Results: ID may be regarded not as a disease or as a disability but as a syndrome grouping (metasyndrome) similar to the construct of dementia. It includes a heterogeneous group of clinical conditions, ranging from genetic to nutritional, infectious, metabolic or neurotoxic conditions. The ID metasyndrome is characterized by a deficit in cognitive functioning prior to the acquisition of skills through learning. The intensity of the deficit is such to interfere in a significant way with individual normal functioning as expressed in limitations in activities and restriction in participation (disabilities).

Conclusions: The name 'developmental cognitive impairment' is here suggested to coexist with ID for naming the metasyndrome previously called MR following a polysemic-polynomious approach.

Citing Articles

Autistic features in patients with intellectual disability attending the psychiatry outpatient department of a tertiary healthcare center.

Akash N, Santre M, Panse S, Madhur R, Sonawane K Ind Psychiatry J. 2024; 33(Suppl 1):S72-S76.

PMID: 39534158 PMC: 11553612. DOI: 10.4103/ipj.ipj_128_24.


Genetic etiology of adult intellectual disability (ID) of unknown cause in Qatar: a retrospective study.

Rustom H, Eltorki Y, Khoodoruth M, Abdallah O, Al-Khuzaei N, Iqbal N Qatar Med J. 2022; 2022(1):26.

PMID: 35756865 PMC: 9197721. DOI: 10.5339/qmj.2022.26.


Evaluating, Filtering and Clustering Genetic Disease Cohorts Based on Human Phenotype Ontology Data with Cohort Analyzer.

Rojano E, Cordoba-Caballero J, Jabato F, Gallego D, Serrano M, Perez B J Pers Med. 2021; 11(8).

PMID: 34442375 PMC: 8398478. DOI: 10.3390/jpm11080730.


Identification and characterization of a missense mutation in the -linked β--acetylglucosamine (-GlcNAc) transferase gene that segregates with X-linked intellectual disability.

Vaidyanathan K, Niranjan T, Selvan N, Teo C, May M, Patel S J Biol Chem. 2017; 292(21):8948-8963.

PMID: 28302723 PMC: 5448127. DOI: 10.1074/jbc.M116.771030.


Advances in understanding - genetic basis of intellectual disability.

Chiurazzi P, Pirozzi F F1000Res. 2016; 5.

PMID: 27127621 PMC: 4830215. DOI: 10.12688/f1000research.7134.1.