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Aetiologic spectrum of mental retardation & developmental delay in India

BACKGROUND & OBJECTIVES: The aetiology of mental retardation is varied and difficult to establish. Reports from India on the spectrum of underlying causative conditions are lacking. This retrospective study was conducted to establish the various aetiologies of mental retardation (MR) and develop...

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Autores principales: Aggarwal, Shagun, Bogula, Vijay Raju, Mandal, Kausik, Kumar, Rashmi, Phadke, Shubha R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510890/
https://www.ncbi.nlm.nih.gov/pubmed/23041737
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author Aggarwal, Shagun
Bogula, Vijay Raju
Mandal, Kausik
Kumar, Rashmi
Phadke, Shubha R.
author_facet Aggarwal, Shagun
Bogula, Vijay Raju
Mandal, Kausik
Kumar, Rashmi
Phadke, Shubha R.
author_sort Aggarwal, Shagun
collection PubMed
description BACKGROUND & OBJECTIVES: The aetiology of mental retardation is varied and difficult to establish. Reports from India on the spectrum of underlying causative conditions are lacking. This retrospective study was conducted to establish the various aetiologies of mental retardation (MR) and developmental delay (DD) in patients attending a medical genetics centre in north India and to assess the contribution of genetic disorders. METHODS: This retrospective study was conducted at a tertiary care centre in north India. All patients attending the centre with MR or DD from January 2007 to December 2009 were included. The aetiology of MR/DD was ascertained after clinical assessment and targeted laboratory evaluation. The spectrum of causative conditions and contribution of genetic disorders was established. RESULTS: A total of 338 patients were included in the study, of whom definite diagnosis was established in 253 (74.8%). The various aetiological categories were: chromosomal disorders in 112 (33.1%), non chromosomal syndromes in 32 (9.5%), neurometabolic disorders in 34 (10.1%), central nervous system structural defects in 25 (7.4%), cerebral palsy in 43 (12.7%) and environmental insults in 7 (2%). Eighty five patients (25.2%) had idiopathic mental retardation. A total of 196 (58%) patients had a genetic disorder as the cause of MR/DD. INTERPRETATION & CONCLUSIONS: The aetiology of MR/DD is varied and difficult to establish in a significant proportion of patients. Chromosomal and various monogenic disorders contribute to a large number of MR/DD cases and hence a genetic work up is essential for all such patients.
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spelling pubmed-35108902012-12-05 Aetiologic spectrum of mental retardation & developmental delay in India Aggarwal, Shagun Bogula, Vijay Raju Mandal, Kausik Kumar, Rashmi Phadke, Shubha R. Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The aetiology of mental retardation is varied and difficult to establish. Reports from India on the spectrum of underlying causative conditions are lacking. This retrospective study was conducted to establish the various aetiologies of mental retardation (MR) and developmental delay (DD) in patients attending a medical genetics centre in north India and to assess the contribution of genetic disorders. METHODS: This retrospective study was conducted at a tertiary care centre in north India. All patients attending the centre with MR or DD from January 2007 to December 2009 were included. The aetiology of MR/DD was ascertained after clinical assessment and targeted laboratory evaluation. The spectrum of causative conditions and contribution of genetic disorders was established. RESULTS: A total of 338 patients were included in the study, of whom definite diagnosis was established in 253 (74.8%). The various aetiological categories were: chromosomal disorders in 112 (33.1%), non chromosomal syndromes in 32 (9.5%), neurometabolic disorders in 34 (10.1%), central nervous system structural defects in 25 (7.4%), cerebral palsy in 43 (12.7%) and environmental insults in 7 (2%). Eighty five patients (25.2%) had idiopathic mental retardation. A total of 196 (58%) patients had a genetic disorder as the cause of MR/DD. INTERPRETATION & CONCLUSIONS: The aetiology of MR/DD is varied and difficult to establish in a significant proportion of patients. Chromosomal and various monogenic disorders contribute to a large number of MR/DD cases and hence a genetic work up is essential for all such patients. Medknow Publications & Media Pvt Ltd 2012-09 /pmc/articles/PMC3510890/ /pubmed/23041737 Text en Copyright: © The Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Aggarwal, Shagun
Bogula, Vijay Raju
Mandal, Kausik
Kumar, Rashmi
Phadke, Shubha R.
Aetiologic spectrum of mental retardation & developmental delay in India
title Aetiologic spectrum of mental retardation & developmental delay in India
title_full Aetiologic spectrum of mental retardation & developmental delay in India
title_fullStr Aetiologic spectrum of mental retardation & developmental delay in India
title_full_unstemmed Aetiologic spectrum of mental retardation & developmental delay in India
title_short Aetiologic spectrum of mental retardation & developmental delay in India
title_sort aetiologic spectrum of mental retardation & developmental delay in india
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510890/
https://www.ncbi.nlm.nih.gov/pubmed/23041737
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