Ectodermal, Skeletal, and Genitourinary Abnormalities With Neonatal Hyperekplexia - 02/08/11
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, Anne Marie Santilli, BS , Jennifer Stone, MS, CGC †, Rhonda E. Schnur, MD † Division of Neurology, Department of Pediatrics, Robert Wood Johnson School of Medicine, and Children’s Regional Hospital and Cooper University Hospital, Camden, New Jersey Communication should be addressed to: Dr. McAbee; Division of Child Neurology; New Jersey Neuroscience Institute and JFK Medical Center; 65 James Street; Edison, NJ 08818.Abstract |
A new syndrome of the major form of hyperekplexia with neonatal onset is described. An infant manifested multisystem involvement with ectodermal anomalies, including lymphedema and double eyelashes (lymphedema-distichiasis syndrome), genitourinary anomalies, and skeletal dysplasia. Despite extensive genetic evaluation, no cytogenetic or molecular etiologies were identified. The literature was reviewed to assess other unusual neurologic and nonneurologic features that have been reported in association with neonatal-onset hyperekplexia—that is, hyperekplexia-plus syndromes.
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Vol 44 - N° 5
P. 381-384 - mai 2011 Retour au numéro
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