Literature DB >> 8281279

Cornelia de Lange syndrome--photo essay.

M Ireland, J Burn.   

Abstract

Cornelia de Lange syndrome is a rare developmental malformation syndrome characterized by developmental delay, retardation of growth, limb reduction abnormalities and dysmorphic facial features. With the exception of one case with a de novo translocation (Ireland et al., 1991) there are no consistent chromosomal abnormalities or biochemical markers. Diagnosis is therefore dependent on the recognition of the distinctive facial features. In this photo essay we focus on those features which are most specific to the syndrome and highlight possible diagnostic pitfalls.

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Year:  1993        PMID: 8281279

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  9 in total

1.  De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes.

Authors:  J E Allanson; R C Hennekam; M Ireland
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey.

Authors:  Sarika Rohatgi; Dinah Clark; Antonie D Kline; Laird G Jackson; Juan Pie; Victoria Siu; Feliciano J Ramos; Ian D Krantz; Matthew A Deardorff
Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

3.  Neuroimaging features of Cornelia de Lange syndrome.

Authors:  Matthew T Whitehead; Usha D Nagaraj; Phillip L Pearl
Journal:  Pediatr Radiol       Date:  2015-02-21

4.  Total hip reconstruction in a woman with Cornelia de Lange syndrome: a case report.

Authors:  R E Grant; J A Schneider; E J Ferguson; P B Cummings
Journal:  J Natl Med Assoc       Date:  1997-08       Impact factor: 1.798

5.  Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome.

Authors:  Maninder Kaur; Cheryl DeScipio; Jennifer McCallum; Dinah Yaeger; Marcella Devoto; Laird G Jackson; Nancy B Spinner; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2005-09-15       Impact factor: 2.802

6.  Cornelia de lange syndrome.

Authors:  Naeimeh Tayebi
Journal:  Indian J Hum Genet       Date:  2008-01

7.  Limb reduction defects in the northern region of England 1985-92.

Authors:  M J Wright; J N Newell; M E Charlton; E N Hey; L J Donaldson; J Burn
Journal:  J Epidemiol Community Health       Date:  1995-06       Impact factor: 3.710

8.  A case of Cornelia de Lange syndrome from Sudan.

Authors:  Mona Ellaithi; David Gisselsson; Therese Nilsson; Atif Elagib; Imad Fadl-Elmula; Mashair Abdelgadir
Journal:  BMC Pediatr       Date:  2007-01-29       Impact factor: 2.125

9.  Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome.

Authors:  Fengchang Qiao; Cuiping Zhang; Yan Wang; Gang Liu; Binbin Shao; Ping Hu; Zhengfeng Xu
Journal:  Front Genet       Date:  2021-02-09       Impact factor: 4.599

  9 in total

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