{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T16:16:32Z","timestamp":1780330592841,"version":"3.54.1"},"reference-count":22,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,6,22]]},"DOI":"10.7759\/cureus.62901","type":"journal-article","created":{"date-parts":[[2024,6,22]],"date-time":"2024-06-22T12:05:41Z","timestamp":1719057941000},"source":"Crossref","is-referenced-by-count":1,"title":["Role of Physiotherapy in Pediatric Lissencephaly: A Case Report and Therapeutic Insights"],"prefix":"10.7759","author":[{"given":"Anam R","family":"Sasun","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H V","family":"Sharath","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.38245","article-title":"Lissencephaly: expanded imaging and clinical classification","volume":"173","author":"Di Donato N","year":"2017","unstructured":"Di Donato N, Chiari S, Mirzaa GM, et al.. Lissencephaly: expanded imaging and clinical classification. Am J Med Genet A. 2017, 173:1473-88. 10.1002\/ajmg.a.38245","journal-title":"Am J Med Genet A"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1016\/j.bpobgyn.2016.10.005","article-title":"Fetal cytomegalovirus infection","volume":"38","author":"Leruez-Ville M","year":"2017","unstructured":"Leruez-Ville M, Ville Y. Fetal cytomegalovirus infection. Best Pract Res Clin Obstet Gynaecol. 2017, 38:97-107. 10.1016\/j.bpobgyn.2016.10.005","journal-title":"Best Pract Res Clin Obstet Gynaecol"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/aws019","article-title":"A developmental and genetic classification for malformations of cortical development: update 2012","volume":"135","author":"Barkovich AJ","year":"2012","unstructured":"Barkovich AJ, Guerrini R, Kuzniecky RI, Jackson GD, Dobyns WB. A developmental and genetic classification for malformations of cortical development: update 2012. Brain. 2012, 135:1348-69. 10.1093\/brain\/aws019","journal-title":"Brain"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1146\/annurev-pathmechdis-012418-012927","article-title":"Malformations of cerebral cortex development: molecules and mechanisms","volume":"14","author":"Juric-Sekhar G","year":"2019","unstructured":"Juric-Sekhar G, Hevner RF. Malformations of cerebral cortex development: molecules and mechanisms. Annu Rev Pathol. 2019, 14:293-318. 10.1146\/annurev-pathmechdis-012418-012927","journal-title":"Annu Rev Pathol"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1186\/s12887-022-03595-6","article-title":"Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report","volume":"22","author":"Simoes C","year":"2022","unstructured":"Simoes C, Gra\u00f1a M, Rodriguez S, et al.. Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report. BMC Pediatr. 2022, 22:545. 10.1186\/s12887-022-03595-6","journal-title":"BMC Pediatr"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.31729\/jnma.7893","article-title":"Lissencephaly with congenital hypothyroidism: a case report","volume":"60","author":"Sahani SK","year":"2022","unstructured":"Sahani SK, Pathak A, Nepali B, Rai N. Lissencephaly with congenital hypothyroidism: a case report. JNMA J Nepal Med Assoc. 2022, 60:978-81. 10.31729\/jnma.7893","journal-title":"JNMA J Nepal Med Assoc"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1111\/j.0013-9580.2005.461010.x","article-title":"Genetic malformations of the cerebral cortex and epilepsy","volume":"46 Suppl 1","author":"Guerrini R","year":"2005","unstructured":"Guerrini R. Genetic malformations of the cerebral cortex and epilepsy. Epilepsia. 2005, 46 Suppl 1:32-7. 10.1111\/j.0013-9580.2005.461010.x","journal-title":"Epilepsia"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/s0035-3787(07)90460-9","article-title":"Genetic and clinical aspects of lissencephaly","volume":"163","author":"Verloes A","year":"2007","unstructured":"Verloes A, Elmaleh M, Gonzales M, Laquerriere A, Gressens P. Genetic and clinical aspects of lissencephaly. Rev Neurol. 2007, 163:533-47. 10.1016\/s0035-3787(07)90460-9","journal-title":"Rev Neurol"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddg086","article-title":"Lissencephaly and the molecular basis of neuronal migration","volume":"12 Spec No 1","author":"Kato M","year":"2003","unstructured":"Kato M, Dobyns WB. Lissencephaly and the molecular basis of neuronal migration. Hum Mol Genet. 2003, 12 Spec No 1:R89-96. 10.1093\/hmg\/ddg086","journal-title":"Hum Mol Genet"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1038\/s41582-020-0395-6","article-title":"International consensus recommendations on the diagnostic work-up for malformations of cortical development","volume":"16","author":"Oegema R","year":"2020","unstructured":"Oegema R, Barakat TS, Wilke M, et al.. International consensus recommendations on the diagnostic work-up for malformations of cortical development. Nat Rev Neurol. 2020, 16:618-35. 10.1038\/s41582-020-0395-6","journal-title":"Nat Rev Neurol"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1055\/s-0036-1582126","article-title":"Prenatal diagnosis of lissencephaly type 2 using three-dimensional ultrasound and fetal MRI: case report and review of the literature","volume":"38","author":"Tonni G","year":"2016","unstructured":"Tonni G, Pattacini P, Bonasoni MP, Araujo J\u00fanior E. Prenatal diagnosis of lissencephaly type 2 using three-dimensional ultrasound and fetal MRI: case report and review of the literature. Rev Bras Ginecol Obstet. 2016, 38:201-6. 10.1055\/s-0036-1582126","journal-title":"Rev Bras Ginecol Obstet"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1080\/09638288.2023.2206164","article-title":"Diagnosis and referrals to physical therapy among caregivers of children with genetic disorders: a qualitative inquiry","volume":"46","author":"Gmmash A","year":"2024","unstructured":"Gmmash A, Alsobhi M, Alzahrani NM, Balamash LM, Alsubhi RM, Almaddah M. Diagnosis and referrals to physical therapy among caregivers of children with genetic disorders: a qualitative inquiry. Disabil Rehabil. 2024, 46:1815-24. 10.1080\/09638288.2023.2206164","journal-title":"Disabil Rehabil"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.7759\/cureus.47863","article-title":"Overview of genetics and role of the pediatric physical therapist in the diagnostic process","volume":"15","author":"Srushti Sudhir C","year":"2023","unstructured":"Srushti Sudhir C, Sharath HV. Overview of genetics and role of the pediatric physical therapist in the diagnostic process. Cureus. 2023, 15:e47863. 10.7759\/cureus.47863","journal-title":"Cureus"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.3390\/jcm10122589","article-title":"Role and effects of hippotherapy in the treatment of children with cerebral palsy: a systematic review of the literature","volume":"10","author":"Menor-Rodr\u00edguez MJ","year":"2021","unstructured":"Menor-Rodr\u00edguez MJ, Sevilla Mart\u00edn M, S\u00e1nchez-Garc\u00eda JC, Montiel-Troya M, Cort\u00e9s-Mart\u00edn J, Rodr\u00edguez-Blanque R. Role and effects of hippotherapy in the treatment of children with cerebral palsy: a systematic review of the literature. J Clin Med. 2021, 10:10.3390\/jcm10122589","journal-title":"J Clin Med"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1016\/j.siny.2021.101272","article-title":"Neonatal encephalopathy: etiologies other than hypoxic-ischemic encephalopathy","volume":"26","author":"Sandoval Karamian AG","year":"2021","unstructured":"Sandoval Karamian AG, Mercimek-Andrews S, Mohammad K, et al.. Neonatal encephalopathy: etiologies other than hypoxic-ischemic encephalopathy. Semin Fetal Neonatal Med. 2021, 26:101272. 10.1016\/j.siny.2021.101272","journal-title":"Semin Fetal Neonatal Med"},{"key":"ref16","doi-asserted-by":"publisher","DOI":"10.1002\/14651858.CD011937.pub2","article-title":"Neurodevelopmental treatment approaches for children with cerebral palsy","volume":"2018","author":"Zanon MA","year":"2018","unstructured":"Zanon MA, Porf\u00edrio GJ, Riera R, Martimbianco AL. Neurodevelopmental treatment approaches for children with cerebral palsy. Cochrane Database Syst Rev. 2018, 2018:CD011937. 10.1002\/14651858.CD011937.pub2","journal-title":"Cochrane Database Syst Rev"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.3390\/biom10060964","article-title":"Reelin functions, mechanisms of action and signaling pathways during brain development and maturation","volume":"10","author":"Jossin Y","year":"2020","unstructured":"Jossin Y. Reelin functions, mechanisms of action and signaling pathways during brain development and maturation. Biomolecules. 2020, 10:10.3390\/biom10060964","journal-title":"Biomolecules"},{"key":"ref18","doi-asserted-by":"publisher","DOI":"10.1002\/ccr3.4882","article-title":"A prenatal case of lissencephaly with cerebellar hypoplasia: new mutation in RELN gene","volume":"9","author":"Balza C","year":"2021","unstructured":"Balza C, Garofalo G, Cos T, et al.. A prenatal case of lissencephaly with cerebellar hypoplasia: new mutation in RELN gene. Clin Case Rep. 2021, 9:e04882. 10.1002\/ccr3.4882","journal-title":"Clin Case Rep"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.1017\/cjn.2016.271","article-title":"Malformations of cortical development: from postnatal to fetal imaging","volume":"43","author":"Lerman-Sagie T","year":"2016","unstructured":"Lerman-Sagie T, Leibovitz Z. Malformations of cortical development: from postnatal to fetal imaging. Can J Neurol Sci. 2016, 43:611-8. 10.1017\/cjn.2016.271","journal-title":"Can J Neurol Sci"},{"key":"ref20","doi-asserted-by":"publisher","DOI":"10.3138\/ptc-2019-0043","article-title":"Do paediatric physiotherapists promote community based physical activity for children and youth with disabilities? A mixed methods study","volume":"73","author":"Shannon J","year":"2021","unstructured":"Shannon J, Legg D, Pritchard-Wiart L. Do paediatric physiotherapists promote community based physical activity for children and youth with disabilities? A mixed methods study. Physiother Can. 2021, 73:66-75. 10.3138\/ptc-2019-0043","journal-title":"Physiother Can"},{"key":"ref21","doi-asserted-by":"publisher","DOI":"10.1097\/MS9.0000000000000176","article-title":"Rare manifestations of alobar holoprosencephaly and the potential causes: a report of two cases","volume":"85","author":"Nakawa W","year":"2023","unstructured":"Nakawa W, Alkhalil S, Martini N, Alawad I. Rare manifestations of alobar holoprosencephaly and the potential causes: a report of two cases. Ann Med Surg (Lond). 2023, 85:252-6. 10.1097\/MS9.0000000000000176","journal-title":"Ann Med Surg (Lond)"},{"key":"ref22","doi-asserted-by":"publisher","DOI":"10.1186\/s12887-016-0731-6","article-title":"Interventions to improve gross motor performance in children with neurodevelopmental disorders: a meta-analysis","volume":"16","author":"Lucas BR","year":"2016","unstructured":"Lucas BR, Elliott EJ, Coggan S, Pinto RZ, Jirikowic T, McCoy SW, Latimer J. Interventions to improve gross motor performance in children with neurodevelopmental disorders: a meta-analysis. BMC Pediatr. 2016, 16:193. 10.1186\/s12887-016-0731-6","journal-title":"BMC Pediatr"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/262759-role-of-physiotherapy-in-pediatric-lissencephaly-a-case-report-and-therapeutic-insights","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,6,22]],"date-time":"2024-06-22T12:05:45Z","timestamp":1719057945000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/262759-role-of-physiotherapy-in-pediatric-lissencephaly-a-case-report-and-therapeutic-insights"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,6,22]]},"references-count":22,"URL":"https:\/\/doi.org\/10.7759\/cureus.62901","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,6,22]]}}}