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Unilateral condylar hyperplasia in hemifacial hyperplasia, is there genetic proof of overgrowth?
Nolte, J W; Alders, M; Karssemakers, L H E; Becking, A G; Hennekam, R C M.
Afiliação
  • Nolte JW; Department of Oral and Maxillofacial Surgery, Amsterdam UMC/Emma Children's Hospital, and Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam, Amsterdam, The Netherlands. Electronic address: j.w.nolte@amc.nl.
  • Alders M; Laboratory of Genome Diagnostics, Amsterdam UMC, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development, Amsterdam, The Netherlands.
  • Karssemakers LHE; Department of Oral and Maxillofacial Surgery, Amsterdam UMC/Emma Children's Hospital, and Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam, Amsterdam, The Netherlands.
  • Becking AG; Department of Oral and Maxillofacial Surgery, Amsterdam UMC/Emma Children's Hospital, and Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam, Amsterdam, The Netherlands; Department of Oral and Maxillofacial Surgery, Spaarne Gasthuis, Haarlem, The Netherlands.
  • Hennekam RCM; Department of Paediatrics and Translational Genetics, Amsterdam UMC/Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
Int J Oral Maxillofac Surg ; 49(11): 1464-1469, 2020 Nov.
Article em En | MEDLINE | ID: mdl-32249036
ABSTRACT
Hemifacial hyperplasia (HFH) is characterized by an increase in volume of all affected tissues of half of the face. It is present at birth, subsequently grows proportionally, and stops growing before adulthood. Unilateral condylar hyperplasia (UCH) consists of progressive asymmetric growth of the mandible and develops typically in early adulthood. Both disorders have an unknown aetiology. The overgrowth limited to one body part suggests somatic mosaicism, as this has been found in other similar localized overgrowth disorders. Often this includes a variant in a gene in the (PIK3CA)/PI3K/(PTEN)/AKT1/mTOR pathway. Here we report the case of an HFH patient with asymmetry present at birth, in whom a progressive growth pattern similar to UCH subsequently occurred, causing marked mandibular asymmetry. A condylectomy was successfully performed to stop the progressive growth. Somatic mosaicism for a mutation in PIK3CA was detected in the condylar tissue. This finding might indicate that both HFH and UCH can be caused by variants in genes in the (PIK3CA)/PI3K/(PTEN)/AKT1/mTOR pathway, similar to other disorders that result in asymmetrical bodily overgrowth.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Assimetria Facial / Côndilo Mandibular Limite: Adult / Humans Idioma: En Revista: Int J Oral Maxillofac Surg Assunto da revista: ODONTOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Assimetria Facial / Côndilo Mandibular Limite: Adult / Humans Idioma: En Revista: Int J Oral Maxillofac Surg Assunto da revista: ODONTOLOGIA Ano de publicação: 2020 Tipo de documento: Article