Literature DB >> 8074145

Severe spondylocostal dysostosis associated with other congenital anomalies: a clinical/epidemiologic analysis and description of ten cases from the Spanish registry.

M L Martínez-Frías1, E Bermejo, L Paisán, M Martín, J Egüés, J A López, S Martínez, C Orbea, F Cucalón, J M Gairi.   

Abstract

We describe 10 cases born to nondiabetic mothers who presented with severe spondylocostal dysostosis (SCD) associated with other anomalies, identified among 20,526 malformed liveborn infants from the Spanish Collaborative Study of Congenital Malformations (ECEMC). We analyze the associated malformations in the 10 cases with severe SCD, as well as in all cases with less severe SCD among children with MCA patterns of unknown cause. Cases with SCD were preferentially associated with caudal dysgenesis, diaphragmatic hernia, and central nervous system anomalies.

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Year:  1994        PMID: 8074145     DOI: 10.1002/ajmg.1320510306

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


  8 in total

Review 1.  The mouse notches up another success: understanding the causes of human vertebral malformation.

Authors:  Duncan B Sparrow; Gavin Chapman; Sally L Dunwoodie
Journal:  Mamm Genome       Date:  2011-06-11       Impact factor: 2.957

2.  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

Review 3.  Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

Authors:  Barbara R Pober
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

4.  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

Review 5.  Molecular genetics of congenital diaphragmatic defects.

Authors:  Malgorzata Bielinska; Patrick Y Jay; Jonathan M Erlich; Susanna Mannisto; Zsolt Urban; Markku Heikinheimo; David B Wilson
Journal:  Ann Med       Date:  2007       Impact factor: 4.709

6.  Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs.

Authors:  Cali E Willet; Mariano Makara; George Reppas; George Tsoukalas; Richard Malik; Bianca Haase; Claire M Wade
Journal:  PLoS One       Date:  2015-02-06       Impact factor: 3.240

7.  Congenital hemangioma in spondylocostal dysostosis: a novel association.

Authors:  Victor Michael Salinas-Torres
Journal:  An Bras Dermatol       Date:  2016 Sep-Oct       Impact factor: 1.896

8.  Spondylocostal Dysostosis: A Literature Review and Case Report with Long-Term Follow-Up of a Conservatively Managed Patient.

Authors:  Brendan R Southam; Adam P Schumaier; Alvin H Crawford
Journal:  Case Rep Orthop       Date:  2018-03-22
  8 in total

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