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Morphological appearance and chemical composition of enamel in primary teeth from patients with 22q11 deletion syndrome.

Klingberg, Gunilla, 1960 (författare)
Gothenburg University,Göteborgs universitet,Odontologiska institutionen, Avdelningen för pedodonti,Institute of Odontology, Department of Pedodontics
Dietz, Wolfram (författare)
Oskarsdóttir, Sólveig, 1953 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa, Avdelningen för pediatrik,Institute for the Health of Women and Children, Dept of Paediatrics
visa fler...
Odelius, Hans, 1943 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för fysik (GU),Department of Physics (GU)
Gelander, Lars, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa,Institute for the Health of Women and Children
Norén, Jörgen G, 1947 (författare)
Gothenburg University,Göteborgs universitet,Odontologiska institutionen, Avdelningen för pedodonti,Institute of Odontology, Department of Pedodontics
visa färre...
 (creator_code:org_t)
Wiley, 2005
2005
Engelska.
Ingår i: European journal of oral sciences. - : Wiley. - 0909-8836 .- 1600-0722. ; 113:4, s. 303-11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Patients with 22q11 deletion syndrome have many and complex medical problems, including hypocalcemia and/or hypoparathyroidism. Odontological findings include enamel aberrations in both dentitions. In order to describe enamel morphology, chemical composition in primary teeth, and to investigate the relationship between medical history and morphological appearance, dental enamel was investigated in 38 exfoliated primary teeth from 15 children and adolescents. Morphology was studied by the use of a polarized light microscope, microradiography, scanning electron microscopy, X-ray microanalysis, and secondary ion mass spectrometry. The morphological findings were compared with medical history. The teeth showed, in principle, a normal morphological appearance with regard to prism structure. A high frequency of aberrations, such as hypomineralization, hypoplasia and extra incremental lines, were found. The majority of the aberrations were found around the neonatal line. There was a relationship between high numbers of medical problems in the patients and enamel deviations. The result supports the hypothesis of under-reporting of both hypocalcemia and hypoparathyroidism in patients with 22q11 deletion syndrome.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Odontologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dentistry (hsv//eng)

Nyckelord

Adolescent
Adult
Child
Child
Preschool
Chromosome Deletion
Chromosomes
Human
Pair 22
genetics
Dental Enamel
abnormalities
chemistry
Female
Humans
Hypocalcemia
complications
genetics
Hypothyroidism
complications
genetics
Male
Severity of Illness Index
Syndrome
Tooth Abnormalities
complications
genetics
Tooth
Deciduous
chemistry
pathology

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