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Acta Odontologica Scandinavica Volume 70, 2012 - Issue 3
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Original Article

Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions?

Hilde Nordgarden National Resource Centre for Oral Health in Rare Medical Conditions (TAKO-centre), Lovisenberg Diakonale Hospital, Oslo, NorwayCorrespondence[email protected]
,
Kari LimaDepartment of Endocrinology, Division of Medicine, Akerhus University Hospital, Lørenskog, Norway;Institute of Clinical Medicine, University of Oslo, Akershus University Hospital, Lørenskog, Norway; Section for Pediatric Immunology and Infectious Diseases, Division of Pediatrics, Oslo University Hospital, Oslo, Norway
,
Nina Skogedal National Resource Centre for Oral Health in Rare Medical Conditions (TAKO-centre), Lovisenberg Diakonale Hospital, Oslo, Norway
,
Ivar FøllingDepartment of Endocrinology, Division of Medicine, Akerhus University Hospital, Lørenskog, Norway
,
Kari Storhaug National Resource Centre for Oral Health in Rare Medical Conditions (TAKO-centre), Lovisenberg Diakonale Hospital, Oslo, Norway
&
Tore G. Abrahamsen Section for Pediatric Immunology and Infectious Diseases, Division of Pediatrics, Oslo University Hospital, Oslo, Norway; Faculty Division Rikshospitalet University Hospital, University of Oslo, Oslo, Norway
Pages 194-201 | Received 17 Nov 2010, Accepted 29 May 2011, Published online: 10 Nov 2011

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Estephania Candelo, Maria Alejandra Estrada-Mesa, Adriana Jaramillo, Carlos Humberto Martinez-Cajas, Julio Cesar Osorio & Harry Pachajoa. (2021) The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report. The Application of Clinical Genetics 14, pages 267-277.
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Articles from other publishers (22)

Erik Boot, Sólveig Óskarsdóttir, Joanne C.Y. Loo, Terrence Blaine Crowley, Ani Orchanian-Cheff, Danielle M. Andrade, Jill M. Arganbright, René M. Castelein, Christine Cserti-Gazdewich, Steven de Reuver, Ania M. Fiksinski, Gunilla Klingberg, Anthony E. Lang, Maria R. Mascarenhas, Edward M. Moss, Beata Anna Nowakowska, Erwin Oechslin, Lisa Palmer, Gabriela M. Repetto, Nikolai Gil D. Reyes, Maude Schneider, Candice Silversides, Kathleen E. Sullivan, Ann Swillen, Therese A.M.J. van Amelsvoort, Jason P. Van Batavia, Claudia Vingerhoets, Donna M. McDonald-McGinn & Anne S. Bassett. (2023) Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine 25:3, pages 100344.
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Sólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, Joanne C.Y. Loo, Jill M. Arganbright, Marco Armando, Adriane L. Baylis, Elemi J. Breetvelt, René M. Castelein, Madeline Chadehumbe, Christopher M. Cielo, Steven de Reuver, Stephan Eliez, Ania M. Fiksinski, Brian J. Forbes, Emily Gallagher, Sarah E. Hopkins, Oksana A. Jackson, Lorraine Levitz-Katz, Gunilla Klingberg, Michele P. Lambert, Bruno Marino, Maria R. Mascarenhas, Julie Moldenhauer, Edward M. Moss, Beata Anna Nowakowska, Ani Orchanian-Cheff, Carolina Putotto, Gabriela M. Repetto, Erica Schindewolf, Maude Schneider, Cynthia B. Solot, Kathleen E. Sullivan, Ann Swillen, Marta Unolt, Jason P. Van Batavia, Claudia Vingerhoets, Jacob Vorstman, Anne S. Bassett & Donna M. McDonald-McGinn. (2023) Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome. Genetics in Medicine 25:3, pages 100338.
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Ana Laura Herrera FarhaRenato Assis MachadoLucimara Teixeira Das NevesRua Sílvio Marchione. (2022) ORAL CONDITIONS AND DENTAL PHENOTYPES IN SUBJECTS WITH PIERRE ROBIN SYNDROMIC SEQUENCE: LITERATURE REVIEW. INDIAN JOURNAL OF APPLIED RESEARCH, pages 46-48.
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Cynthia B. Solot. 2022. The Chromosome 22q11.2 Deletion Syndrome. The Chromosome 22q11.2 Deletion Syndrome 286 301 .
Deborah H. Wong, Sadna Rajan, Kerrod B. Hallett & David J. Manton. (2021) Medical and dental characteristics of children with chromosome 22q11.2 deletion syndrome at the Royal Children's Hospital, Melbourne. International Journal of Paediatric Dentistry 31:6, pages 682-690.
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Brianne B. Roby, Michael Broderick & Lauren A. Bohm. 2021. Cummings Pediatric Otolaryngology. Cummings Pediatric Otolaryngology 154 163 .
Theodosia Bartzela. 2021. Fundamentals of Craniofacial Malformations. Fundamentals of Craniofacial Malformations 271 297 .
Sha Yu, Wen‐xia Chen, Wei Lu, Chao Chen, Yihua Ni, Bo Duan, Bin Wang, Huijun Wang & Zheng‐min Xu. (2020) Novel heterozygous GATA3 and SLC34A3 variants in a 6‐year‐old boy with Barakat syndrome and hypercalciuria . Molecular Genetics & Genomic Medicine 8:5.
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M. A. Dolgikh, M. A. Bolkov, I. A. Tuzankina, N. G. Sarkisyan & N. A. Hovsepyan. (2019) Oral manifestations of primary immunodeficiencies. Bulletin of Siberian Medicine 18:3, pages 144-154.
Crossref
Tine B. Sivertsen, Anne N. Åstrøm, Gottfried Greve, Jörg Aßmus & Marit S. Skeie. (2018) Effectiveness of an oral health intervention program for children with congenital heart defects. BMC Oral Health 18:1.
Crossref
Mohammed Ali AlQarni, Adel Alharbi & Leena Merdad. (2018) Dental management of a patient with 22q11.2 deletion syndrome (22q11.2DS). BMJ Case Reports, pages bcr-2018-225765.
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J. Greenwall-Cohen, L. Greenwall, V. Haywood & K. Harley. (2018) Tooth whitening for the under-18-year-old patient. British Dental Journal 225:1, pages 19-26.
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Jane Hejlesen, Line Underbjerg, Hans Gjørup, Agnes Bloch-Zupan, Tanja Sikjaer, Lars Rejnmark & Dorte Haubek. (2018) Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review. Frontiers in Physiology 9.
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Hans Gjørup, Signe Sparre Beck-Nielsen & Dorte Haubek. (2017) Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemia. Clinical Oral Investigations 22:2, pages 745-755.
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Theodosia N. Bartzela, Carine Carels & Jaap C. Maltha. (2017) Update on 13 Syndromes Affecting Craniofacial and Dental Structures. Frontiers in Physiology 8.
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ME Peacock, RM Arce & CW Cutler. (2016) Periodontal and other oral manifestations of immunodeficiency diseases. Oral Diseases 23:7, pages 866-888.
Crossref
S. Gao, M. Moreno, S. Eliason, H. Cao, X. Li, W. Yu, F. B. Bidlack, H. C. Margolis, A. Baldini & B. A. Amendt. (2015) TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome. Human Molecular Genetics 24:8, pages 2330-2348.
Crossref
Mike Harrison, Angus Cameron & Nicky Kilpatrick. 2015. Planning and Care for Children and Adolescents with Dental Enamel Defects. Planning and Care for Children and Adolescents with Dental Enamel Defects 45 58 .
WK Seow. (2014) Developmental defects of enamel and dentine: challenges for basic science research and clinical management. Australian Dental Journal 59, pages 143-154.
Crossref
Shan Gao, Xiao Li & Brad A. Amendt. (2013) Understanding the Role of Tbx1 as a Candidate Gene for 22q11.2 Deletion Syndrome. Current Allergy and Asthma Reports 13:6, pages 613-621.
Crossref
S Salanitri & WK Seow. (2013) Developmental enamel defects in the primary dentition: aetiology and clinical management. Australian Dental Journal 58:2, pages 133-140.
Crossref
Barbara TYMCZYNA, Marcin R. TATARA, Witold KRUPSKI, Monika TYMCZYNA-SOBOTKA & Teresa BACHANEK. (2013) Interrelationships between Tooth Properties and Biochemical Bone Turnover Markers Investigated on Six-Month-Old Pig Model. Journal of Veterinary Medical Science 75:3, pages 269-274.
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