Literature DB >> 1501958

Platyspondylic lethal osteochondrodysplasia: Shiraz type with radiological-pathological correlation.

R S Campbell1, M Ireland, C A Bloxham, A J Chippindale.   

Abstract

We report two cases of a platyspondylic lethal osteochondrodysplasia in siblings. The condition affects predominantly the metaphyses of the axial skeleton associated with limb shortening and mild platyspondyly. The radiological and pathological features correlate very closely with Sedaghatian's lethal metaphyseal chondrodysplasia, which has previously been described only in Iranian Nationals. Both the radiological and pathological appearances will be described, together with a discussion of the differential diagnosis, the genetical implications and a review of literature.

Entities:  

Mesh:

Year:  1992        PMID: 1501958     DOI: 10.1007/bf02011302

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  6 in total

1.  Further heterogeneity within lethal neonatal short-limbed dwarfism: the platyspondylic types.

Authors:  W A Horton; D L Rimoin; D W Hollister; R S Lachman
Journal:  J Pediatr       Date:  1979-05       Impact factor: 4.406

2.  Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms.

Authors:  M D Fallon; S L Teitelbaum; R S Weinstein; S Goldfischer; D M Brown; M P Whyte
Journal:  Medicine (Baltimore)       Date:  1984-01       Impact factor: 1.889

3.  Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant?

Authors:  R M Winter; E M Thompson
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.

Authors:  J M Opitz; J W Spranger; H R Stöss; H J Pesch; B Azadeh
Journal:  Am J Med Genet       Date:  1987-03

5.  Congenital lethal metaphyseal chondrodysplasia: a newly recognized complex autosomal recessive disorder.

Authors:  M R Sedaghatian
Journal:  Am J Med Genet       Date:  1980

Review 6.  Radiologic nosology of bone dysplasias.

Authors:  J Spranger
Journal:  Am J Med Genet       Date:  1989-09
  6 in total
  1 in total

1.  The Shwachman-Bodian-Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type.

Authors:  Gen Nishimura; Eiji Nakashima; Yuichiro Hirose; Trevor Cole; Phillip Cox; Daniel H Cohn; David L Rimoin; Ralph S Lachman; Yoshinari Miyamoto; Bronwyn Kerr; Sheila Unger; Hirofumi Ohashi; Andrea Superti-Furga; Shiro Ikegawa
Journal:  J Med Genet       Date:  2007-04       Impact factor: 6.318

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.