Literature DB >> 8279481

Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna.

P Beighton1, E Sujansky, B Patzak, K A Portele.   

Abstract

Skeletal material in the Museum of Pathological Anatomy, Vienna, has been appraised in order to modify existing descriptive designations and to establish diagnoses of specific genetic disorders. In this way osseous material relating to classical genetic syndromes has been identified and will be available for further study. Among the skeletons of adults in the museum, the following genetic conditions could be diagnosed: achondroplasia, Marfan syndrome, cleidocranial dysostosis, and diaphyseal aclasia. In adult sisters with dwarfism and a rickety bone disorder, the final diagnosis was uncertain. Infantile bone dysplasias, genetic conditions involving the skull, and malformation syndromes which are all represented in the museum are currently being analyzed.

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Year:  1993        PMID: 8279481     DOI: 10.1002/ajmg.1320470609

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  [Surgical treatment of cardiovascular manifestations of Marfan's syndrome].

Authors:  R Lange; E Ebert
Journal:  Herz       Date:  1999-12       Impact factor: 1.443

2.  [Karl Alfons Portele, Pathologist and first director of the Federal Pathologic-anatomical Museum Vienna].

Authors:  Beatrix Patzak; Eduard Winter
Journal:  Wien Med Wochenschr       Date:  2013-07-16

3.  Cleidocranial dysplasia: complete clinical, radiological and histological profiles.

Authors:  Ruchieka Vij; Puneet Batra; Hitesh Vij
Journal:  BMJ Case Rep       Date:  2013-03-20

4.  Bone dysplasias of infancy in the Vienna collection.

Authors:  P Beighton; E Sujansky; B Patzak; K A Portele
Journal:  Pediatr Radiol       Date:  1994

Review 5.  Radiological imaging of teratological fetuses: what can we learn?

Authors:  Lucas L Boer; A N Schepens-Franke; J J A van Asten; D G H Bosboom; K Kamphuis-van Ulzen; T L Kozicz; D J Ruiter; R-J Oostra; W M Klein
Journal:  Insights Imaging       Date:  2017-04-24

6.  Detection of G1138A Mutation of the FGFR3 Gene in Tooth Material from a 180-Year-Old Museological Achondroplastic Skeleton.

Authors:  Lucas L Boer; Jana Naue; Laurens de Rooy; Roelof-Jan Oostra
Journal:  Genes (Basel)       Date:  2017-08-29       Impact factor: 4.096

  6 in total

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