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Callosal anomalies with interhemispheric cyst: Expanding the phenotype

✍ Scribed by Piero Pavone; Rita Barone; Sabrina Baieli; Enrico Parano; Gemma Incorpora; Martino Ruggieri


Book ID
114814464
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
274 KB
Volume
94
Category
Article
ISSN
0803-5253

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## Abstract Oculoectodermal syndrome (OES, OMIM 600268) is characterized by discrete areas of alopecia of the scalp and epibulbar dermoids which are present from birth, with additional variable anomalies. We describe two patients, one of whom has been reported [Lees et al. (2000); Am J Med Genet 91

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## Abstract ## BACKGROUND Methotrexate (MTX) embryopathy was described nearly 50 years ago, when this agent began to be used as a cancer treatment and abortifacient. In this report we describe a case with typical features of MTX syndrome together with new features to expand the phenotype. ## CASE