Literature DB >> 1856834

Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency.

I M Buntinx1, P J Willems, S E Spitaels, P J Van Reempst, A M De Paepe, J E Dumon.   

Abstract

We describe a male neonate with severe arachnodactyly, hypermobility of the fingers, flexion contractures of elbows, wrists, hips, and knees, micrognathia, crumpled ears, rockerbottom feet, loose redundant skin, and ocular abnormalities. Severe cardiac valve insufficiency and aortic dilatation resulted in cardiac failure and death 20 hours after birth. This case represents the severe end of the clinical spectrum of Marfan syndrome. As similar patients have been reported, they may represent a separate mutation.

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Year:  1991        PMID: 1856834      PMCID: PMC1016831          DOI: 10.1136/jmg.28.4.267

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


  25 in total

1.  Arachnodactyly associated with aneurysm of the aorta.

Authors:  H S TRAISMAN; F R JOHNSON
Journal:  AMA Am J Dis Child       Date:  1954-02

2.  Segregation of all four major fibrillar collagen genes in the Marfan syndrome.

Authors:  D J Ogilvie; B P Wordsworth; L M Priestley; R Dalgleish; J Schmidtke; B Zoll; B C Sykes
Journal:  Am J Hum Genet       Date:  1987-12       Impact factor: 11.025

3.  First International Symposium on the Marfan syndrome. July 8-10, 1988, Baltimore, Maryland. Abstracts.

Authors: 
Journal:  Am J Med Genet       Date:  1989-02

4.  Congenital contractural arachnodactyly. A heritable disorder of connective tissue.

Authors:  R K Beals; F Hecht
Journal:  J Bone Joint Surg Am       Date:  1971-07       Impact factor: 5.284

5.  Mitral valve disease in Marfan's syndrome.

Authors:  N Marlow; J E Gregg; S A Qureshi
Journal:  Arch Dis Child       Date:  1987-09       Impact factor: 3.791

6.  International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986.

Authors:  P Beighton; A de Paepe; D Danks; G Finidori; T Gedde-Dahl; R Goodman; J G Hall; D W Hollister; W Horton; V A McKusick
Journal:  Am J Med Genet       Date:  1988-03

7.  Pulmonary hyperinflation and emphysema in infants with the Marfan syndrome.

Authors:  R Dominguez; R A Weisgrau; M Santamaria
Journal:  Pediatr Radiol       Date:  1987

8.  Pulmonary emphysema in a neonate with Marfan syndrome.

Authors:  D L Day; B A Burke
Journal:  Pediatr Radiol       Date:  1986

9.  Severe perinatal Marfan syndrome.

Authors:  D M Gross; L K Robinson; L T Smith; N Glass; H Rosenberg; M Duvic
Journal:  Pediatrics       Date:  1989-07       Impact factor: 7.124

10.  Probable homozygotic form of the Marfan syndrome in a newborn child.

Authors:  J Schollin; B Bjarke; K H Gustavson
Journal:  Acta Paediatr Scand       Date:  1988-05
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  13 in total

1.  Evolving phenotype of Marfan's syndrome.

Authors:  K J Lipscomb; J Clayton-Smith; R Harris
Journal:  Arch Dis Child       Date:  1997-01       Impact factor: 3.791

Review 2.  Marfan syndrome in the third Millennium.

Authors:  Gwenaëlle Collod-Béroud; Catherine Boileau
Journal:  Eur J Hum Genet       Date:  2002-11       Impact factor: 4.246

3.  Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndrome.

Authors:  M Godfrey; M Raghunath; J Cisler; C L Bevins; A DePaepe; M Di Rocco; J Gregoritch; K Imaizumi; P Kaplan; Y Kuroki
Journal:  Am J Pathol       Date:  1995-06       Impact factor: 4.307

4.  An unusual patient with the neonatal Marfan phenotype and mitochondrial complex I deficiency.

Authors:  J Christodoulou; R Petrova-Benedict; B H Robinson; V Jay; J T Clarke
Journal:  Eur J Pediatr       Date:  1993-05       Impact factor: 3.183

5.  Prenatal congenital vertical talus (rocker bottom foot): a marker for multisystem anomalies.

Authors:  Eva I Rubio; Nimisha Mehta; Anna R Blask; Dorothy I Bulas
Journal:  Pediatr Radiol       Date:  2017-09-06

6.  Histone Deacetylase 3 Coordinates Deacetylase-independent Epigenetic Silencing of Transforming Growth Factor-β1 (TGF-β1) to Orchestrate Second Heart Field Development.

Authors:  Sara L Lewandowski; Harish P Janardhan; Chinmay M Trivedi
Journal:  J Biol Chem       Date:  2015-09-29       Impact factor: 5.157

7.  A group of patients with Marfan's syndrome, who have finger and toe contractures, displays tendons' alterations upon an ultrasound examination: are these features common among classical Marfan patients?

Authors:  Daniela Melchiorre; Elisa Pratelli; Elena Torricelli; Francesco Sofi; Rosanna Abbate; Marco Matucci-Cerinic; GianFranco Gensini; Guglielmina Pepe
Journal:  Intern Emerg Med       Date:  2016-02-22       Impact factor: 3.397

8.  A compound-heterozygous Marfan patient: two defective fibrillin alleles result in a lethal phenotype.

Authors:  L Karttunen; M Raghunath; L Lönnqvist; L Peltonen
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

9.  Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome.

Authors:  A Superti-Furga; M Raghunath; P J Willems
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

10.  Dilatation of the great arteries in an infant with marfan syndrome and ventricular septal defect.

Authors:  L Rozendaal; N A Blom; Y Hilhorst-Hofstee; A D J Ten Harkel
Journal:  Case Rep Med       Date:  2011-07-12
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