{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:20:45Z","timestamp":1761718845910},"reference-count":14,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2010,9,1]],"date-time":"2010-09-01T00:00:00Z","timestamp":1283299200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Epileptic Disorders"],"published-print":{"date-parts":[[2010,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>Epilepsy is the most common and serious neurological symptom in ring chromosome 14 syndrome, also characterised by mild dysmorphisms, acquired microcephaly, cognitive impairment, hypotonia and ocular abnormalities. Typically, early\u2010onset, polymorphous and drug\u2010resistant seizures are reported. Status epilepticus has not been previously reported. We describe a nine\u2010year\u2010old Caucasian boy with ring 14 syndrome who presented a severe early\u2010onset and drug\u2010resistant focal epilepsy with secondary generalised seizures and repetitive episodes of convulsive and non\u2010convulsive status epilepticus. The electro\u2010clinical evaluation of prolonged seizures and their long\u2010term consequences is important for the practical management of these patients and for a better comprehension of the syndrome.<\/jats:p>","DOI":"10.1684\/epd.2010.0324","type":"journal-article","created":{"date-parts":[[2019,8,2]],"date-time":"2019-08-02T13:24:19Z","timestamp":1564752259000},"page":"222-227","source":"Crossref","is-referenced-by-count":11,"title":["Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome"],"prefix":"10.1002","volume":"12","author":[{"given":"Simona","family":"Giovannini","sequence":"first","affiliation":[{"name":"Neuropsichiatria Infantile Ospedale Maggiore Bologna Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniele","family":"Frattini","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Arcispedale S. Maria Nuova Reggio Emilia Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Angela","family":"Scarano","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Arcispedale S. Maria Nuova Reggio Emilia Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carlo","family":"Fusco","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Arcispedale S. Maria Nuova Reggio Emilia Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gianna","family":"Bertani","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Arcispedale S. Maria Nuova Reggio Emilia Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elvio Della","family":"Giustina","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Arcispedale S. 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Maria Nuova Reggio Emilia Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniela","family":"Orteschi","sequence":"additional","affiliation":[{"name":"Istituto di Genetica Medica Universit\u00e0 Cattolica del Sacro Cuore Roma Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marcella","family":"Zollino","sequence":"additional","affiliation":[{"name":"Istituto di Genetica Medica Universit\u00e0 Cattolica del Sacro Cuore Roma Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giovanni","family":"Neri","sequence":"additional","affiliation":[{"name":"Istituto di Genetica Medica Universit\u00e0 Cattolica del Sacro Cuore Roma Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giuseppe","family":"Gobbi","sequence":"additional","affiliation":[{"name":"Neuropsichiatria Infantile Ospedale Maggiore Bologna Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2010,9]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.0013-9580.2005.02804.x"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1528-1167.2007.01345.x"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1177\/155005940503600305"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1528-1157.2003.05403.x"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0887-8994(98)00099-X"},{"key":"e_1_2_4_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.seizure.2007.08.004"},{"key":"e_1_2_4_8_1","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1684\/epd.2007.0121","article-title":"Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome","volume":"9","author":"Ricard\u2010Mousnier B","year":"2007","journal-title":"Epileptic Disord"},{"key":"e_1_2_4_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30942"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0387-7604(12)80243-9"},{"key":"e_1_2_4_11_1","first-page":"68","article-title":"Complex partial status epilepticus","volume":"34","author":"Treiman DM","year":"1983","journal-title":"Adv Neurol"},{"key":"e_1_2_4_12_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10207"},{"key":"e_1_2_4_13_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1469-8749.2009.03292.x"},{"key":"e_1_2_4_14_1","first-page":"93","article-title":"Ring chromosome 14 syndrome. 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