Literature DB >> 4002008

Cardiac defects in a patient with congenital contractural arachnodactyly.

R E Bell, J J Wheller.   

Abstract

Congenital contractural arachnodactyly (CCA) is a connective tissue disorder sharing many of the clinical manifestations of Marfan's syndrome. The case presented emphasizes that severe cardiac involvement may be manifested in the neonate with CCA, thus altering the more characteristic benign prognosis of CCA.

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Year:  1985        PMID： 4002008     DOI： 10.1097/00007611-198506000-00032

Source DB:  PubMed          Journal:  South Med J        ISSN： 0038-4348            Impact factor:   0.954


  3 in total

1.  Cardiac anomalies complicating congenital contractural arachnodactyly.

Authors:  A J Macnab; L D'Orsogna; D E Cole; P E Baguley; R J Adderley; M W Patterson
Journal:  Arch Dis Child       Date:  1991-10       Impact factor: 3.791

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

Authors:  I M Buntinx; P J Willems; S E Spitaels; P J Van Reempst; A M De Paepe; J E Dumon
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

3.  Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound.

Authors:  Ryuta Miyake; Mayuko Ichikawa; Katsuhiko Naruse
Journal:  BMJ Case Rep       Date:  2021-03-01
  3 in total

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