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Patients with <jats:italic>CLDN1<\/jats:italic>\u00a0mutations, and specifically \u00ab\u00a0the Moroccan\u00bb c.200_201delTT deletion, may be an increased risk for neurodevelopmental symptoms such as learning disabilities, mental retardation, and language delay.<\/jats:p>","DOI":"10.1111\/pde.14976","type":"journal-article","created":{"date-parts":[[2022,3,19]],"date-time":"2022-03-19T00:44:00Z","timestamp":1647650640000},"page":"590-593","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Evaluation of neurodevelopmental symptoms in 10 cases of neonatal ichthyosis and sclerosing cholangitis syndrome"],"prefix":"10.1111","volume":"39","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6687-5497","authenticated-orcid":false,"given":"Deborah","family":"Salik","sequence":"first","affiliation":[{"name":"Department of Dermatology H\u00f4pital Universitaire des Enfants Reine Fabiola Universit\u00e9 Libre de Bruxelles 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