Long-term survival in a child with severe congenital contractural arachnodactyly, autism and severe intellectual disability

Katie M.G. Snape, Michael C. Fahey, George McGillivray, Prateek Gupta, Dianna M. Milewicz, Martin B. Delatycki

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2 Citations (Scopus)

Abstract

The severe form of congenital contractural arachnodactyly is usually associated with early mortality due to multisystem complications. Here, we report a 9-year-old male child with severe skeletal manifestations of congenital contractural arachnodactyly. He had none of the cardiovascular or gastrointestinal features that have been described in severe congenital contractural arachnodactyly. He had profound intellectual disability with autism. All exons of FBN2, the gene associated with congenital contractural arachnodactyly, were sequenced and no disease-causing mutation was found. When severe congenital contractural arachnodactyly is diagnosed in the newborn period, parents need to be aware that long-term survival is possible, particularly if no significant extraskeletal complications are present, and that significant neurodevelopmental delay may occur.

Original languageEnglish
Pages (from-to)95-99
Number of pages5
JournalClinical Dysmorphology
Volume15
Issue number2
DOIs
Publication statusPublished - 1 Apr 2006
Externally publishedYes

Keywords

  • Beals syndrome
  • Lehal disorder
  • Neonatal Marfan syndrome

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