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Congenital disorder of glycosylation IIa: The trouble with diagnosing a dysmorphic inborn error of metabolism

Authors

  • Anas M. Alazami,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • Dorota Monies,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • Brian F. Meyer,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • Fatema Alzahrani,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • Mais Hashem,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • Mustafa A. Salih,

    1. Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia
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  • Fowzan S. Alkuraya

    Corresponding author
    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    2. Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia
    3. Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
    • Developmental Genetics Unit, King Faisal Specialist Hospital and Research Center, MBC-03, PO Box 3354, Riyadh 11211, Saudi Arabia.
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  • How to cite this article: Alazami AM, Monies D, Meyer BF, Alzahrani F, Hashem M, Saleh M, Alkuraya FS. 2012. Congenital disorder of glycosylation IIa: The trouble with diagnosing a dysmorphic inborn error of metabolism. Am J Med Genet Part A 158A:245–246.

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