{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,9,8]],"date-time":"2024-09-08T07:39:23Z","timestamp":1725781163640},"reference-count":23,"publisher":"Walter de Gruyter GmbH","issue":"1","license":[{"start":{"date-parts":[[2017,7,20]],"date-time":"2017-07-20T00:00:00Z","timestamp":1500508800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2017,7,20]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Congenital Myasthenic Syndrome (CMS) is a group of inherited neuromuscular junction disorders caused by defects in several genes. Clinical features include delayed motor milestones, recurrent respiratory illnesses and variable fatigable weakness. The central nervous system involvement is typically not part of the CMS. We report here a Saudi girl with genetically proven Collagen Like Tail Subunit Of Asymmetric Acetylcholinesterase (COLQ) mutation type CMS who has global developmental delay, microcephaly and respiratory failure. We have reviewed the literature regarding COLQ-type CMS and to the best of our knowledge this is the first ever reported association of congenital myasthenia syndrome with microcephaly.<\/jats:p>","DOI":"10.1515\/tnsci-2017-0011","type":"journal-article","created":{"date-parts":[[2017,7,21]],"date-time":"2017-07-21T10:01:18Z","timestamp":1500631278000},"source":"Crossref","is-referenced-by-count":2,"title":["COLQ-mutant congenital myasthenic syndrome with microcephaly: A unique case with literature review"],"prefix":"10.1515","volume":"8","author":[{"given":"Sulaiman Bazee","family":"Al-Mobarak","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammad A.","family":"Al-Muhaizea","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","reference":[{"key":"ref71","first-page":"11","article-title":"Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary","volume":"61","year":"2008","journal-title":"Ideggyogy Sz."},{"key":"ref211","doi-asserted-by":"crossref","first-page":"699","DOI":"10.1007\/s12098-008-0132-4","article-title":"Neuromuscular junctional disorders","volume":"75","year":"2008","journal-title":"Indian J. 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