{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,6]],"date-time":"2026-04-06T15:04:06Z","timestamp":1775487846532,"version":"3.50.1"},"reference-count":17,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2008,9,29]],"date-time":"2008-09-29T00:00:00Z","timestamp":1222646400000},"content-version":"vor","delay-in-days":4016,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Develop Med Child Neuro"],"published-print":{"date-parts":[[1997,10]]},"abstract":"<jats:p>Foix\u2010Chavany\u2010Marie syndrome (FCMS) is characterized by facio\u2010linguo\u2010masticatory diplegia in the absence of limb weakness. The most common cause is a cortical lesion resulting from a stroke but a congenital form has been reported. We present the case of a 53\u2010year\u2010old man who was admitted to hospital with worsening dysphagia which was know to have been present together with anarthria and facial palsy, since birth. He demonstrated features of FCMS with pseudobulbar palsy and unaffected reflexes and automatic responses. Cranial CT and MRI scans showed bilateral opercular lesions of CSF intensity in continuity with the lateral ventricles. We conclude that this case of static FCMS for over SO years may represent a \u2018pure\u2019 form of congenital FCMS with motor symptomatology and unaccompanied by mental retardation or epilepsy.<\/jats:p>","DOI":"10.1111\/j.1469-8749.1997.tb07366.x","type":"journal-article","created":{"date-parts":[[2010,7,16]],"date-time":"2010-07-16T12:33:32Z","timestamp":1279283612000},"page":"696-698","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Pure congenital Foix\u2010Chavany\u2010Marie syndrome"],"prefix":"10.1111","volume":"39","author":[{"given":"P.","family":"Nisipeanu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Rieder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Blamen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amos D.","family":"Korczyn","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2008,9,29]]},"reference":[{"key":"e_1_2_1_2_1","first-page":"441","article-title":"La diplegie faciale cerebrale (forme corticale de la paralysie pseudobulbaire)","volume":"40","author":"Alajouanine T.","year":"1933","journal-title":"Revue Neurologique"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410250115"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1991.00530170061021"},{"key":"e_1_2_1_5_1","first-page":"770","volume-title":"Handbook of Clinical Neurology. 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