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Coronary Artery Abnormalities in Hyper-IgE Syndrome

✍ Scribed by Alexandra F. Freeman; Elizabeth Mannino Avila; Pamela A. Shaw; Joie Davis; Amy P. Hsu; Pamela Welch; Jatin R. Matta; Colleen Hadigan; Roderic I. Pettigrew; Steven M. Holland; Ahmed M. Gharib

Publisher
Springer
Year
2011
Tongue
English
Weight
409 KB
Volume
31
Category
Article
ISSN
0271-9142

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A 9-year-old boy with hyperimmunoglobulin-E-syndrome (HIE) and craniosynostosis is reported. Premature fusion of the sagittal and lambdoid suture led to scaphocephaly. A partial optic atrophy without clinical signs of raised intracranial pressure was observed. This is the fourth reported case of cra