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Delleman Syndrome A Case Report with Emphasis on Neuroimaging

Author

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  • Husain Naser

    (Department of Radiology, Salmaniya Medical complex, Bahrain)

Abstract

Delleman syndrome, also called Oculocerebrocutaneous syndrome (OCCS) is a rare congenital sporadic disorder that appears at birth. The syndrome is characterised primarily by a triad of eye, brain and skin malformations given its name “Oculocerebrocutaneous†syndrome. The diagnosis is confirmed by brain MRI with a malformation involving mainly the forebrain and mid-hindbrain. To date, about 40 patients have been reported by OCCS. We present a case with the typical neuroimaging feature of a patient with OCCS.

Suggested Citation

  • Husain Naser, 2018. "Delleman Syndrome A Case Report with Emphasis on Neuroimaging," International Journal of Cell Science & Molecular Biology, Juniper Publishers Inc., vol. 3(5), pages 80-81, January.
    • Handle: RePEc:adp:ijcsmb:v:3:y:2018:i:5:p:80-81
    DOI: 10.19080/IJCSMB.2018.03.555622
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