Literature DB >> 3236365

Congenital spinal deformity in a three generation family.

I K Temple1, T G Thomas, M Baraitser.   

Abstract

Short stature resulting from spinal deformity in three generations of a family is reported. Multiple vertebral anomalies were found in the proband and are the probable underlying cause of the severe scoliosis seen in the adult members. The pattern of inheritance suggests that an autosomal dominant gene is responsible for this condition, but it may well be the same gene that causes the dominant form of spondylocostal dysostosis, this family representing one end of the spectrum with mild rib changes. The clinical features of spondylocostal dysostosis are reviewed.

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Year:  1988        PMID: 3236365      PMCID: PMC1051611          DOI: 10.1136/jmg.25.12.831

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  11 in total

1.  [Polydysspondylic syndrome due to 14-15 translocation and dyschondrosteosis in the same subject. Familial segregation].

Authors:  J C MLYNARSKI; P MAROTEAUX; G DESHAIES; C BENICHOU; C SALMON
Journal:  C R Hebd Seances Acad Sci       Date:  1963-02-11

2.  Occipito-facial-cervico-thoracic-abdomino-digital dysplasia; Jarcho-Levin syndrome of vertebral anomalies. Report of six cases and review of the literature.

Authors:  A Pérez-Comas; J M García-Castro
Journal:  J Pediatr       Date:  1974-09       Impact factor: 4.406

3.  Spondylo-thoracic dysplasia in three sisters.

Authors:  I P Castroviejo; T Rodriguez-Costa; F Castillo
Journal:  Dev Med Child Neurol       Date:  1973-06       Impact factor: 5.449

4.  The autosomal recessive form of spondylocostal dysostosis.

Authors:  P Franceschini; E Grassi; C Fabris; G Bogetti; M Randaccio
Journal:  Radiology       Date:  1974-09       Impact factor: 11.105

5.  Spondylocostal dysplasia. A dominantly inherited form of short-trunked dwarfism.

Authors:  D L Rimoin; B D Fletcher; V A McKusick
Journal:  Am J Med       Date:  1968-12       Impact factor: 4.965

6.  Second trimester prenatal diagnosis of the Jarcho-Levin syndrome.

Authors:  J L Tolmie; M J Whittle; M B McNay; A A Gibson; J M Connor
Journal:  Prenat Diagn       Date:  1987-02       Impact factor: 3.050

7.  Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica.

Authors:  R Wynne-Davies
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

8.  Spondylocostal/spondylothoracic dysostosis: the clinical basis for prognosticating and genetic counseling.

Authors:  S Aymé; M Preus
Journal:  Am J Med Genet       Date:  1986-08

9.  Hereditary costovertebral dysplasia with malignant cerebral tumour.

Authors:  T J David; A Glass
Journal:  J Med Genet       Date:  1983-12       Impact factor: 6.318

10.  Spondylocostal dysostosis in South African sisters.

Authors:  P Beighton; F T Horan
Journal:  Clin Genet       Date:  1981-01       Impact factor: 4.438

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  4 in total

1.  A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Authors:  P D Turnpenny; M P Bulman; T M Frayling; T K Abu-Nasra; C Garrett; A T Hattersley; S Ellard
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.

Authors:  P D Turnpenny; N Whittock; J Duncan; S Dunwoodie; K Kusumi; S Ellard
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

3.  Evidence for variable gene expression in a large inbred kindred with autosomal recessive spondylocostal dysostosis.

Authors:  P D Turnpenny; R J Thwaites; F N Boulos
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

4.  Five known tagging DLL3 SNPs are not associated with congenital scoliosis: A case-control association study in a Chinese Han population.

Authors:  Yong Yang; Bing-Qiang Wang; Zhi-Hong Wu; Hai-Yan Zhang; Gui-Xing Qiu; Jian-Xiong Shen; Jian-Guo Zhang; Yu Zhao; Yi-Peng Wang; Qi Fei
Journal:  Medicine (Baltimore)       Date:  2016-07       Impact factor: 1.889

  4 in total

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