{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:12:48Z","timestamp":1761718368426},"reference-count":20,"publisher":"FapUNIFESP (SciELO)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Arq. Neuro-Psiquiatr."],"published-print":{"date-parts":[[2015,1]]},"abstract":"<jats:p>ObjectiveTo present a seven-cases serie of Mowat-Wilson syndrome (MWS).MethodAll patients with positive mutation for the ZEB2 were evaluated by a geneticist and a neurologist, with clinical and laboratorial characterization.ResultsA peculiar facies and mental retardation were present in all patients. The Denver II scale showed intense delay in all aspects, especially fine motor and adaptive. Acquired microcephaly was observed in five patients. Only one patient did not present epilepsy. Epilepsy was focal and predominating in sleep, with status epilepticus in three patients. The initial seizure was associated with fever in most patients (4\/6). The EEG showed epileptic focal activity (5\/7). The imaging studies revealed total agenesis (4\/7) and partial agenesis of the corpus callosum (1\/7).ConclusionPhysicians who care for patients with mental retardation and epilepsy should be aware of SMW.<\/jats:p>","DOI":"10.1590\/0004-282x20140182","type":"journal-article","created":{"date-parts":[[2015,1,17]],"date-time":"2015-01-17T20:45:58Z","timestamp":1421527558000},"page":"12-17","source":"Crossref","is-referenced-by-count":14,"title":["Mowat-Wilson syndrome: neurological and molecular study in seven patients"],"prefix":"10.1590","volume":"73","author":[{"given":"Jos\u00e9 Albino da","family":"Paz","sequence":"first","affiliation":[{"name":"Universidade de S\u00e3o Paulo, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chong Ae","family":"Kim","sequence":"additional","affiliation":[{"name":"Universidade de S\u00e3o Paulo, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Goossens","sequence":"additional","affiliation":[{"name":"H\u00f4pital Henri Mondor, France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Irina","family":"Giurgea","sequence":"additional","affiliation":[{"name":"H\u00f4pital Henri Mondor, France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria Joaquina","family":"Marques-Dias","sequence":"additional","affiliation":[{"name":"Universidade de S\u00e3o Paulo, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"530","reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1136\/jmg.35.8.617","article-title":"Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23","volume":"35","author":"Mowat DR","year":"1998","journal-title":"J Med 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