A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK

Background: Cleft lip and palate or isolated cleft palate is one of the most common congenital anomalies with a general prevalence of 1 in 700 live births. The aetiology is considered to be a combination of genetic and environmental factors. Clinical genetics service provides information, diagnosis,...

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Main Authors: Rajshree Jayarajan, Pradeep Vasudevan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Journal of Cleft Lip Palate and Craniofacial Anomalies
Subjects:
Online Access:http://www.jclpca.org/article.asp?issn=2348-2125;year=2019;volume=6;issue=2;spage=73;epage=83;aulast=Jayarajan
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spelling doaj-5d880b804b0341acbdb07270f4d53c742021-01-08T04:07:38ZengWolters Kluwer Medknow PublicationsJournal of Cleft Lip Palate and Craniofacial Anomalies2348-21252348-36442019-01-0162738310.4103/jclpca.jclpca_4_19A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UKRajshree JayarajanPradeep VasudevanBackground: Cleft lip and palate or isolated cleft palate is one of the most common congenital anomalies with a general prevalence of 1 in 700 live births. The aetiology is considered to be a combination of genetic and environmental factors. Clinical genetics service provides information, diagnosis, counselling, management and support to patients and families with genetic disorders. Materials and Methods: Data collection was carried out retrospectively from the Genetics department database. The details regarding referrals, assessment, genetic tests and outcomes were analyzed. Results: There were 33 cases from 2012 to 2016. The majority of cases (61%) were White British. Others included Caribbean, Chinese, Indian, Other Asian, and other mixed categories. 67% of patients had associated other anomalies ranging from being part of a syndrome to separate entities. 36% had family history of clefts and 24% of family members had anomalies other than cleft. Genetic analysis showed abnormality only in 4 of the cases (12%) and 2 had results of unknown significance. Conclusions: Genetic counselling should be built into the plan of cleft care in a structured manner and made available to both patients and parents. There should be a global approach to improve identification and analysis of functional elements controlling gene expression. Integration of genetics and environmental risk using epigenetics is warranted so that aetiology can be better defined and eventual outcome would be more effective clinical care and prevention.http://www.jclpca.org/article.asp?issn=2348-2125;year=2019;volume=6;issue=2;spage=73;epage=83;aulast=Jayarajanchromosomal microarraycleft lipcleft palategenetic counselinggenetics
collection DOAJ
language English
format Article
sources DOAJ
author Rajshree Jayarajan
Pradeep Vasudevan
spellingShingle Rajshree Jayarajan
Pradeep Vasudevan
A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
Journal of Cleft Lip Palate and Craniofacial Anomalies
chromosomal microarray
cleft lip
cleft palate
genetic counseling
genetics
author_facet Rajshree Jayarajan
Pradeep Vasudevan
author_sort Rajshree Jayarajan
title A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
title_short A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
title_full A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
title_fullStr A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
title_full_unstemmed A comprehensive review of orofacial cleft patients at a university hospital genetic department in the UK
title_sort comprehensive review of orofacial cleft patients at a university hospital genetic department in the uk
publisher Wolters Kluwer Medknow Publications
series Journal of Cleft Lip Palate and Craniofacial Anomalies
issn 2348-2125
2348-3644
publishDate 2019-01-01
description Background: Cleft lip and palate or isolated cleft palate is one of the most common congenital anomalies with a general prevalence of 1 in 700 live births. The aetiology is considered to be a combination of genetic and environmental factors. Clinical genetics service provides information, diagnosis, counselling, management and support to patients and families with genetic disorders. Materials and Methods: Data collection was carried out retrospectively from the Genetics department database. The details regarding referrals, assessment, genetic tests and outcomes were analyzed. Results: There were 33 cases from 2012 to 2016. The majority of cases (61%) were White British. Others included Caribbean, Chinese, Indian, Other Asian, and other mixed categories. 67% of patients had associated other anomalies ranging from being part of a syndrome to separate entities. 36% had family history of clefts and 24% of family members had anomalies other than cleft. Genetic analysis showed abnormality only in 4 of the cases (12%) and 2 had results of unknown significance. Conclusions: Genetic counselling should be built into the plan of cleft care in a structured manner and made available to both patients and parents. There should be a global approach to improve identification and analysis of functional elements controlling gene expression. Integration of genetics and environmental risk using epigenetics is warranted so that aetiology can be better defined and eventual outcome would be more effective clinical care and prevention.
topic chromosomal microarray
cleft lip
cleft palate
genetic counseling
genetics
url http://www.jclpca.org/article.asp?issn=2348-2125;year=2019;volume=6;issue=2;spage=73;epage=83;aulast=Jayarajan
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