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Major gene and multifactorial inheritance of mandibular prognathism
Mandibular prognathism typically shows familial aggregation. Various genetic models have been described and it is assumed to be a multifactorial and polygenic trait, with a threshold for expression. Our goal was to examine specific genetic models of the familial transmission of this trait. The study...
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Published in: | American journal of medical genetics. Part A 2008-01, Vol.146A (1), p.71-77 |
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container_title | American journal of medical genetics. Part A |
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creator | Cruz, Ricardo Machado Krieger, Henrique Ferreira, Ricardo Mah, James Hartsfield Jr, James Oliveira, Silviene |
description | Mandibular prognathism typically shows familial aggregation. Various genetic models have been described and it is assumed to be a multifactorial and polygenic trait, with a threshold for expression. Our goal was to examine specific genetic models of the familial transmission of this trait. The study sample comprised of 2,562 individuals from 55 families. Complete family histories for each proband were ascertained and the affection status of relatives were confirmed by lateral cephalograms, photographs, and dental models. Pedigrees were drawn using PELICAN and complex segregation analysis was performed using POINTER. Parts of some pedigrees were excluded to create one founder pedigrees, so the total N was 2,050. Analysis showed more affected females than males (P = 0.030). The majority of the pedigrees suggest autosomal dominant inheritance. Incomplete penetrance was demonstrated by the ratio of affected/unaffected parents and siblings. The heritability of mandibular prognathism was estimated to be 0.316. We conclude that there is a major gene that influences the expression of mandibular prognathism with clear signs of Mendelian inheritance and a multifactorial component. © 2007 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ajmg.a.32062 |
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Various genetic models have been described and it is assumed to be a multifactorial and polygenic trait, with a threshold for expression. Our goal was to examine specific genetic models of the familial transmission of this trait. The study sample comprised of 2,562 individuals from 55 families. Complete family histories for each proband were ascertained and the affection status of relatives were confirmed by lateral cephalograms, photographs, and dental models. Pedigrees were drawn using PELICAN and complex segregation analysis was performed using POINTER. Parts of some pedigrees were excluded to create one founder pedigrees, so the total N was 2,050. Analysis showed more affected females than males (P = 0.030). The majority of the pedigrees suggest autosomal dominant inheritance. Incomplete penetrance was demonstrated by the ratio of affected/unaffected parents and siblings. The heritability of mandibular prognathism was estimated to be 0.316. We conclude that there is a major gene that influences the expression of mandibular prognathism with clear signs of Mendelian inheritance and a multifactorial component. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4825</identifier><identifier>EISSN: 1552-4833</identifier><identifier>DOI: 10.1002/ajmg.a.32062</identifier><identifier>PMID: 18074368</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Cephalometry ; Child ; Chromosome Segregation ; Chromosomes, Human ; Dental Models ; Female ; Genes, Dominant ; Humans ; Incidence ; major gene ; Male ; Malocclusion - genetics ; mandibular prognathism ; Medical genetics ; Medical sciences ; Middle Aged ; Models, Genetic ; multifactorial ; Multifactorial Inheritance ; Pedigree ; Penetrance ; Prevalence ; Prognathism - epidemiology ; Prognathism - genetics ; Quantitative Trait, Heritable ; segregation analysis</subject><ispartof>American journal of medical genetics. 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Part A</title><addtitle>Am. J. Med. Genet</addtitle><description>Mandibular prognathism typically shows familial aggregation. Various genetic models have been described and it is assumed to be a multifactorial and polygenic trait, with a threshold for expression. Our goal was to examine specific genetic models of the familial transmission of this trait. The study sample comprised of 2,562 individuals from 55 families. Complete family histories for each proband were ascertained and the affection status of relatives were confirmed by lateral cephalograms, photographs, and dental models. Pedigrees were drawn using PELICAN and complex segregation analysis was performed using POINTER. Parts of some pedigrees were excluded to create one founder pedigrees, so the total N was 2,050. Analysis showed more affected females than males (P = 0.030). The majority of the pedigrees suggest autosomal dominant inheritance. Incomplete penetrance was demonstrated by the ratio of affected/unaffected parents and siblings. The heritability of mandibular prognathism was estimated to be 0.316. We conclude that there is a major gene that influences the expression of mandibular prognathism with clear signs of Mendelian inheritance and a multifactorial component. © 2007 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cephalometry</subject><subject>Child</subject><subject>Chromosome Segregation</subject><subject>Chromosomes, Human</subject><subject>Dental Models</subject><subject>Female</subject><subject>Genes, Dominant</subject><subject>Humans</subject><subject>Incidence</subject><subject>major gene</subject><subject>Male</subject><subject>Malocclusion - genetics</subject><subject>mandibular prognathism</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Models, Genetic</subject><subject>multifactorial</subject><subject>Multifactorial Inheritance</subject><subject>Pedigree</subject><subject>Penetrance</subject><subject>Prevalence</subject><subject>Prognathism - epidemiology</subject><subject>Prognathism - genetics</subject><subject>Quantitative Trait, Heritable</subject><subject>segregation analysis</subject><issn>1552-4825</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp90DlPxDAQBWALgbg7apQGKrL4SGK7hBUsIC4JEKU1SSaLlxxgJwL-PYZdoKOyZX8zT3qE7DA6YpTyQ5g10xGMBKcZXyLrLE15nCghln_vPF0jG97PKBU0ldkqWWOKykRkap2Mr2DWuWiKLUbQllEz1L2toOg7Z6GObPuEzvbQFhh1VdQEYvOhBhe9uG7aQv9kfbNFViqoPW4vzk3ycHpyPz6LL28m5-Ojy7hIMsljLCFnnCuNJQIvKKVaoMzzqhQKAZLwojHPIXzmoLTEUlMQVGFSpFmlldgk-_O9Ift1QN-bxvoC6xpa7AZvJGVZKpkO8GAOC9d577AyL8424D4Mo-arNPNVmgHzXVrgu4u9Q95g-YcXLQWwtwDgC6grF_qw_s9pnSrNRHBi7t5sjR__hpqji6vJT3w8n7K-x_ffKXDPJpNCpubxemIujs9kou-0uRWf9S2VuQ</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Cruz, Ricardo Machado</creator><creator>Krieger, Henrique</creator><creator>Ferreira, Ricardo</creator><creator>Mah, James</creator><creator>Hartsfield Jr, James</creator><creator>Oliveira, Silviene</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080101</creationdate><title>Major gene and multifactorial inheritance of mandibular prognathism</title><author>Cruz, Ricardo Machado ; Krieger, Henrique ; Ferreira, Ricardo ; Mah, James ; Hartsfield Jr, James ; Oliveira, Silviene</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4672-edab12289edea2c00093e7bbfd38eaa4c009ebbaea2ba897ed90a308e4c56f983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cephalometry</topic><topic>Child</topic><topic>Chromosome Segregation</topic><topic>Chromosomes, Human</topic><topic>Dental Models</topic><topic>Female</topic><topic>Genes, Dominant</topic><topic>Humans</topic><topic>Incidence</topic><topic>major gene</topic><topic>Male</topic><topic>Malocclusion - genetics</topic><topic>mandibular prognathism</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Models, Genetic</topic><topic>multifactorial</topic><topic>Multifactorial Inheritance</topic><topic>Pedigree</topic><topic>Penetrance</topic><topic>Prevalence</topic><topic>Prognathism - epidemiology</topic><topic>Prognathism - genetics</topic><topic>Quantitative Trait, Heritable</topic><topic>segregation analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cruz, Ricardo Machado</creatorcontrib><creatorcontrib>Krieger, Henrique</creatorcontrib><creatorcontrib>Ferreira, Ricardo</creatorcontrib><creatorcontrib>Mah, James</creatorcontrib><creatorcontrib>Hartsfield Jr, James</creatorcontrib><creatorcontrib>Oliveira, Silviene</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics. 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Our goal was to examine specific genetic models of the familial transmission of this trait. The study sample comprised of 2,562 individuals from 55 families. Complete family histories for each proband were ascertained and the affection status of relatives were confirmed by lateral cephalograms, photographs, and dental models. Pedigrees were drawn using PELICAN and complex segregation analysis was performed using POINTER. Parts of some pedigrees were excluded to create one founder pedigrees, so the total N was 2,050. Analysis showed more affected females than males (P = 0.030). The majority of the pedigrees suggest autosomal dominant inheritance. Incomplete penetrance was demonstrated by the ratio of affected/unaffected parents and siblings. The heritability of mandibular prognathism was estimated to be 0.316. We conclude that there is a major gene that influences the expression of mandibular prognathism with clear signs of Mendelian inheritance and a multifactorial component. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18074368</pmid><doi>10.1002/ajmg.a.32062</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Cephalometry Child Chromosome Segregation Chromosomes, Human Dental Models Female Genes, Dominant Humans Incidence major gene Male Malocclusion - genetics mandibular prognathism Medical genetics Medical sciences Middle Aged Models, Genetic multifactorial Multifactorial Inheritance Pedigree Penetrance Prevalence Prognathism - epidemiology Prognathism - genetics Quantitative Trait, Heritable segregation analysis |
title | Major gene and multifactorial inheritance of mandibular prognathism |
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