Delleman Oorthuys syndrome: ‘Oculocerebrocutaneous syndrome’
نویسندگان
چکیده
Delleman Oorthuys syndrome (oculocerebrocutaneous syndrome) is a rare, congenital sporadic disorder affecting the skin and central nervous system. We present the case of a one-month-old male who presented with an orbital cyst in the left eye since birth along with other manifestations of this syndrome. The manifestations of this syndrome resemble other developmental disorders like Goldenhar and Goltz syndrome. Conservative management of the orbital cyst in these cases have been described. The need to diagnose this rare congenital anomaly with cerebral malformations as a separate entity is crucial in the management of these children.
منابع مشابه
Delleman syndrome: a case report and review.
A case of oculocerebrocutaneous syndrome is presented, to our knowledge the first to be reported in West Bank and Gaza. The child was of consanguinous parents. The clinical features of orbital cyst, periorbital cutaneous malformations, and cerebral malformations are described, together with a brief review of previous reports. The need for neurological follow-up of these cases is emphasised.
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L I AL-GAZALI*, D DONNAIt, S A BERRYI, B SAY§, AND R F MUELLER* From *the Department of Genetic Counselling, The Clarendon Wing, Leeds General Infirmary, Leeds; tthe Department of Medical Genetics, St Mary's Hospital, Manchester; tthe Division of Genetics, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota; and §the H Allen Chapman Research Institute of Medical Genetics, ...
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