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Journal of Child Neurology
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Marin-Amat Syndrome: Case Report and Review of the Literature

Piero Pavone

Division of Pediatric Neurology University of Catania Catania,, Italy

Rosaria Garozzo

Division of Pediatric Neurology University of Catania Catania,, Italy

Rosario R. Trifiletti

Department of Neurology, Neuroscience and Pediatrics The New York Hospital-Cornell University Medical Center New York, New York

Enrico Parano

Istituto di Bioimmc~gini e Fisiopatologia del Sisteme Nervoso Centrale, Consiglio Nazionale delle Ricerche Catania, Italy

We report a 10-year-old girl with Marin-Amat syndrome, a rare facial synkinesis sometimes referred to as the inverted Marcus Gunn phenomenon. Symptoms were apparent 6 months following unilateral peripheral facial nerve palsy Her facial synkinesis failed to improve, despite improvement in her facial palsy consistent with an aberrant regeneration of the facial nerve. The clinical features of the reported cases of Marin-Amat syndrome are briefly reviewed. To our knowledge, this is the first documented report of Marin-Amat syndrome in a child. ( J Child Neurol 1999; 14:266-267).

Journal of Child Neurology, Vol. 14, No. 4, 266-268 (1999)
DOI: 10.1177/088307389901400411
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A case of familial inverse Marcus Gunn phenomenon
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