Publication:
Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred

dc.contributor.authorsAtasu, M.; Eryilmaz, A.; Genc, A.; Ozcan, M.; Ozbayrak, S.
dc.date.accessioned2022-03-28T12:45:46Z
dc.date.accessioned2026-01-10T18:53:13Z
dc.date.available2022-03-28T12:45:46Z
dc.date.issued1997
dc.description.abstractThe dental, clinical, genetic, radiological and dermatoglyphic findings in patients from a large kindred with congenital hypodontia of maxillary lateral incisors (CHMLI) in association with coloboma of the iris (Cl) and hypomaturation type of amelogenesis imperfecta (HTAI) are presented. The pedigree of the kindred showing multiple consanguinaeous marriages and the findings of the family members with CHMLI and a family member with CHMLI, Cl and HTAI and two members with both CHMLI and HTAI suggested that the isolated CHMLI was due to an autosomal recessive gene, but, the Cl was determined by an autosomal dominant gene linked to CHMLI gene. HTAI was an autosomal recessive character linked to both CHMLI and Cl.
dc.identifier.issn1053-4628
dc.identifier.pubmedPMID: 9484124
dc.identifier.urihttps://hdl.handle.net/11424/255001
dc.language.isoeng
dc.relation.ispartofThe Journal of Clinical Pediatric Dentistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAdult
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectChild
dc.subjectAnodontia
dc.subjectMaxilla
dc.subjectIncisor
dc.subjectAbnormalities, Multiple
dc.subjectColoboma
dc.subjectIris
dc.subjectPedigree
dc.subjectDermatoglyphics
dc.subjectAmelogenesis Imperfecta
dc.subjectGenetic Linkage
dc.subjectGenes, Dominant
dc.titleCongenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage355
oaire.citation.startPage341
oaire.citation.titleThe Journal of Clinical Pediatric Dentistry
oaire.citation.volume4

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