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Skeletal Dysplasia Families: A Stepwise Approach to Diagnosis

Handa, Atsuhiko (författare)
Boston Childrens Hosp, MA 02115 USA
Grigelioniene, Giedre (författare)
Karolinska Institutet,Linköpings universitet,Institutionen för biomedicinska och kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Klinisk genetik,Karolinska Inst, Sweden; Karolinska Univ Hosp, Sweden
Nishimura, Gen (författare)
Karolinska Inst, Sweden; Saitama Univ Hosp, Japan
 (creator_code:org_t)
RADIOLOGICAL SOC NORTH AMERICA (RSNA), 2023
2023
Engelska.
Ingår i: Radiographics. - : RADIOLOGICAL SOC NORTH AMERICA (RSNA). - 0271-5333 .- 1527-1323. ; 43:5
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Skeletal dysplasias are a heterogeneous collection of genetic disorders characterized by bone and cartilage abnormalities, and they encompass over 400 disorders. These disorders are rare individually, but collectively they are common (approximate incidence of one in 5000 births). Radiologists occasionally encounter skeletal dysplasias in daily practice. In the 1980s, Professor Juergen Spranger proposed a concept suitable for the diagnosis of skeletal dysplasias termed bone dysplasia families. He stated that (a) different bone dysplasias that share a similar skeletal pattern can be grouped into a “family,” (b) the final diagnosis is feasible through the provisional recognition of a pattern followed by a more careful analysis, and (c) families of bone dysplasias may be the result of similar pathogenetic mechanisms. The prototypes of bone dysplasia families include dysostosis multiplex family, achondroplasia family, spondyloepiphyseal dysplasia congenita family, and Larsen syndrome–otopalatodigital syndrome family. Since Spranger’s proposal, the concept of bone dysplasia families, along with advancing genetic techniques, has been validated and further expanded. Today, this molecularly proven concept enables a simple stepwise approach to be applied to the radiologic diagnosis of skeletal dysplasias. The first step is the categorization of a given case into a family based on pattern recognition, and the second step is more meticulous observation, such as identification of different severities of the same pattern or subtle but distinctive findings. Since major skeletal dysplasias are limited in number, radiologists can be familiar with the representative patterns of these disorders. The authors describe a stepwise radiologic approach to diagnosing major skeletal dysplasia families and review the clinical and genetic features of these disorders.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Medicinteknik -- Medicinsk bildbehandling (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering -- Medical Image Processing (hsv//eng)

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Av författaren/redakt...
Handa, Atsuhiko
Grigelioniene, G ...
Nishimura, Gen
Om ämnet
TEKNIK OCH TEKNOLOGIER
TEKNIK OCH TEKNO ...
och Medicinteknik
och Medicinsk bildbe ...
Artiklar i publikationen
Radiographics
Av lärosätet
Linköpings universitet
Karolinska Institutet

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