All Relations between Intellectual Disability and cerebellum

Reference Sentence Publish Date Extraction Date Species
Runfeng Zhang, Peng Jia, Yanyi Yao, Feng Zh. Case Report: Identification of a novel Frontiers in genetics vol 13 issue 2022 36092876 case report: identification of a novel mental retardation and microcephaly with pontine and cerebellar hypoplasia (micpch) is a rare genetic disorder that results in varying levels of pontocerebellar hypoplasia, microcephaly, and severe intellectual disabilities. 2022-09-12 2022-09-14 Not clear
Yuta Narishige, Hisao Yaoita, Moriei Shibuya, Miki Ikeda, Kaori Kodama, Aritomo Kawashima, Yukimune Okubo, Wakaba Endo, Takehiko Inui, Noriko Togashi, Soichiro Tanaka, Yasuko Kobayashi, Akira Onuma, Jun Takayama, Gen Tamiya, Atsuo Kikuchi, Shigeo Kure, Kazuhiro Haginoy. Two Siblings with Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome 4 and a Novel Variant of ATP8A2. The Tohoku journal of experimental medicine vol 256 issue 4 2022 35321980 cerebellar ataxia, mental retardation, and disequilibrium syndrome 4 (camrq4) is early onset neuromotor disorder and intellectual disabilities caused by variants of atp8a2. 2022-05-02 2022-05-03 Not clear
Marie Anne-Catherine Neumann, Dajana Grossmann, Simone Schimpf-Linzenbold, Dana Dayan, Katarina Stingl, Reut Ben-Menachem, Ophry Pines, Fran\\xc3\\xa7ois Massart, Sylvie Delcambre, Jenny Ghelfi, Jill Bohler, Tim Strom, Amit Kessel, Abdussalam Azem, Ludger Sch\\xc3\\xb6ls, Anne Gr\\xc3\\xbcnewald, Bernd Wissinger, Rejko Kr\\xc3\\xbcge. Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophy. Scientific reports vol 10 issue 1 2020 33028849 mutations in the aco2 gene were identified in patients suffering from a broad range of symptoms, including optic nerve atrophy, cortical atrophy, cerebellar atrophy, hypotonia, seizures and intellectual disabilities. 2020-12-08 2022-01-14 Not clear
Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Pannee Visrutaratna, Sasitorn Petcharunpaisan, Bruce M Carlson, Worrachet Intachai, Jutamas Sudasna, Jatupol Kampuansai, Prapai Dejkhamro. WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts. Journal of human genetics vol 64 issue 4 2019 30692598 we report an additional case where arachnoid cysts extend the phenotype, and that also confirms the association of intellectual disabilities with asymmetric cerebellar hypoplasia here. 2019-03-14 2022-01-13 Not clear
Robert Savag. Cerebellar tasks do not distinguish between children with developmental dyslexia and children with intellectual disability. Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence vol 13 issue 5 2007 17805993 the present results therefore provide no support for the claim that cerebellar deficits or ran distinguish between children with dyslexia and children with intellectual disabilities that include reading. 2007-12-11 2022-01-12 Not clear
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