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PEER-REVIEWED
Cognitive Study
| Published: March 29, 2020
A study on morphological features in relation with co-morbidities of down ’s syndrome
Post graduate, Department of Anatomy, Guntur medical college, Guntur, India Google Scholar More about the auther
Assistant Professor, Department of Psychiatry, Katuri Medical College, Guntur, India Google Scholar More about the auther
Professor and HOD, Department of Anatomy, Guntur medical college, Guntur, India Google Scholar More about the auther
DIP: 18.01.063/20200801
DOI: 10.25215/0801.063
ABSTRACT
Background: Downs syndrome (DS) is the most commonly identified genetic form of mental retardation and the leading cause of specific birth defects and medical conditions. DS is a multi-system disorder with varied clinical features that affects the individual physically, medically and psychologically. Aims and Objectives:1. To study the morphological features of DS and their co morbidities. 2.To study the relation between morphology and co morbidities of DS. Materials and methods: This were an observational study done at special school for downs syndrome (n= 60). After prior consent socio demographic data was taken using semi structured proforma and morphological data was noted by general examination and the co-morbidities are noted with the clinical reports available with them. Discussion: Morphological features in the current study are varied and supports the earlier literature that DS is a multi-system disorder that affects the individual physically, medically and psychologically. Results: Individuals showed diversified clinical features .Results revealed that males are more than females and among the associated clinical features majority of the individuals have flat nose and least number of individuals have nystagmus. Conclusion: DS is a genetic anomaly with considerable medical co morbidities. Early identification of co morbidities with proper health education to the parents helps in preventing the major harmful effects and promotes better healthier life.
Keywords
Downs syndrome, Trisomy 21, Special children, Genetic disorders
This is an Open Access Research distributed under the terms of the Creative Commons Attribution License (www.creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any Medium, provided the original work is properly cited.
© 2020, M S Madhuri, S Pasupula & P Savithri
Received: January 12, 2020; Revision Received: March 16, 2020; Accepted: March 29, 2020
Article Overview
ISSN 2348-5396
ISSN 2349-3429
18.01.063/20200801
10.25215/0801.063
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Published in Volume 08, Issue 1, January-March, 2020