Literature DB >> 16761119

Spondylocarpotarsal synostosis syndrome: MRI evaluation of vertebral and disk malformation.

Magnus Breitling1, Edmond G Lemire, Michael Rabin.   

Abstract

Spondylocarpotarsal synostosis syndrome (SSS) is a rare autosomal recessive condition characterized primarily by vertebral malsegmentation, carpal/tarsal coalition, and a dysmorphic appearance. Differentiating SSS from other congenital scoliosis syndromes requires evaluation of the vertebrae, ribs, soft tissues, and spinal cord. The enhanced resolution over plain radiographs seen with MRI allows more detailed assessment of vertebral malformation and surrounding anatomy. Diagnosis of the underlying cause of congenital scoliosis might be enhanced using this technology. We report on a 12-year-old girl of unaffected parents with SSS who was evaluated with MRI sequences of the spine to show various types of malsegmentation. Additionally, there is the new finding of fusion of teeth, with developmental failure of a canine incisor.

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Year:  2006        PMID: 16761119     DOI: 10.1007/s00247-006-0181-7

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


  5 in total

Review 1.  Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies.

Authors:  K E Coêlho; E S Ramos; T M Felix; L Martelli; J M de Pina-Neto; N Niikawa
Journal:  Am J Med Genet       Date:  1998-04-28

2.  Spondylocarpotarsal synostosis with epiphyseal dysplasia.

Authors:  Christina Honeywell; Leonard Langer; Judith Allanson
Journal:  Am J Med Genet       Date:  2002-05-15

3.  Spondylocarpotarsal synostosis syndrome (with a posterior midline unsegmented bar).

Authors:  A Al Kaissi; M Ben Ghachem; N Nassib; F Ben Chehida; K Kozlowski
Journal:  Skeletal Radiol       Date:  2004-11-16       Impact factor: 2.199

4.  Spondylocarpotarsal synostosis syndrome and cervical instability.

Authors:  L H Seaver; E Boyd
Journal:  Am J Med Genet       Date:  2000-04-24

5.  A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.

Authors:  C Steiner; N Ehtesham; K D Taylor; E Sebald; R Cantor; L M King; X Guo; T Hang; M S Hu; J-R Cui; B Friedman; D Norato; J Allanson; C Honeywell; G Mettler; F Field; R Lachman; D H Cohn; D Krakow
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

  5 in total
  2 in total

1.  Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model.

Authors:  Jennifer Zieba; Kimberly N Forlenza; Kelly Heard; Jorge H Martin; Michaela Bosakova; Daniel H Cohn; Stephen P Robertson; Pavel Krejci; Deborah Krakow
Journal:  Bone Res       Date:  2022-04-26       Impact factor: 13.362

2.  Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations.

Authors:  Nicola Brunetti-Pierri; Valentina Esposito; Daniele De Brasi; Dario Maria Mattiacci; Deborah Krakow; Brendan Lee; Mariacarolina Salerno
Journal:  Am J Med Genet A       Date:  2008-05-01       Impact factor: 2.802

  2 in total

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