Literature DB >> 3564988

Two hereditary spinal diseases producing kyphosis during adolescence.

O G Nielsen, P Pilgaard.   

Abstract

Familial accumulation of spinal osteochondrosis (Scheuermann's disease) and hereditary juvenile anterior fusion of the vertebral bodies in the thoraco-lumbal area are reported for the first time in the same family. Radiological examination of the spine in 2 planes of 73 persons formed the basis for the study. Nine cases of spinal osteochondrosis and 5 cases of hereditary juvenile anterior fusion were found. Proliferation and increased height of the anterior surface of the body of the vertebrae and pronounced reduction in the anterior aspect of the intervertebral spaces were characteristic during the early stages of the latter condition, similarly fewer back symptoms and a better prognosis were observed in these patients than was the case of patients with Scheuermann's disease.

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Mesh:

Year:  1987        PMID: 3564988     DOI: 10.1111/j.1651-2227.1987.tb10429.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  6 in total

1.  [Hip dysplasia and spinal osteochondritis (Scheuermann's disease) in a girl with type II manifesting collagenopathy].

Authors:  A Al Kaissi; F Laccone; C Karner; R Ganger; K Klaushofer; F Grill
Journal:  Orthopade       Date:  2013-11       Impact factor: 1.087

2.  Dominant inheritance of Scheuermann's juvenile kyphosis.

Authors:  A Findlay; A N Conner; J M Connor
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

3.  Familial Scheuermann disease: a genetic and linkage study.

Authors:  L McKenzie; D Sillence
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

4.  Mice with a targeted deletion of the tetranectin gene exhibit a spinal deformity.

Authors:  K Iba; M E Durkin; L Johnsen; E Hunziker; K Damgaard-Pedersen; H Zhang; E Engvall; R Albrechtsen; U M Wewer
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

5.  Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen-Goldberg syndrome: a report on a family over 4 generations: Case report.

Authors:  Ali Al Kaissi; Zahra Marrakchi; Nabil M Nassib; Jochen Hofstaetter; Franz Grill; Rudolf Ganger; Susanne Gerit Kircher
Journal:  Medicine (Baltimore)       Date:  2017-03       Impact factor: 1.889

Review 6.  The mode of inheritance of Scheuermann's disease.

Authors:  A M Zaidman; M N Zaidman; E L Strokova; A V Korel; E V Kalashnikova; T V Rusova; M V Mikhailovsky
Journal:  Biomed Res Int       Date:  2013-09-12       Impact factor: 3.411

  6 in total

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