WebApr 7, 2024 · Neuroimaging and endocrine disorders in paediatric optic nerve hypoplasia. Br J Ophthalmol. 2024 Jul;102(7):906-910. 4. Parr JR, Dale NJ, Shaffer LM, Salt AT. Social communication difficulties and autism spectrum disorder in young children with optic nerve hypoplasia and/or septo-optic dysplasia. Dev Med Child Neurol. 2010 Oct;52(10):917-21. WebMoreover, other more recently identified associations with optic nerve hypoplasia such as developmental and cognitive delay and relational and communication difficulties and autism may be independent of septum pellucidum development. 121 The extent of pituitary dysfunction in optic nerve hypoplasia patients is highly variable: from short ...
Autism assessment in children with optic nerve hypoplasia …
WebJun 1, 2024 · Optic Nerve Hypoplasia and Autism: Common Features of Spectrum Diseases Reappraisal of the Optic Nerve Hypoplasia Syndrome: Journal of Neuro-Ophthalmology (lww.com) Prevalence and risk factors for disrupted circadian rhythmicity in children with optic nerve hypoplasia – PubMed (nih.gov) WebSep 3, 2013 · The Autism Diagnostic Observation Schedule (ADOS) and the Autism Diagnostic Interview, Revised (ADI-R) were systematically modified and used to assess symptoms of autism in children with vision less than or equal to 20/800, the majority of whom had optic nerve hypoplasia. c言語 while 条件式
Optic Nerve Hypoplasia: Symptoms, Diagnosis & Treatment - All About Vision
WebApr 3, 2024 · Case report review of children with septo-optic dysplasia and optic nerve hypoplasia Reviewed by Claire Howard 3 April 2024 Claire Howard Neuro-Ophthalmology Vision , nystagmus , optic nerve hypoplasia , paediatrics , septo-optic dysplasia , strabismus WebOct 7, 2013 · To report prevalence, ocular characteristics and coexisting behavioural problems in children and adolescents with optic nerve hypoplasia (ONH), which is a common cause of visual impairment in children in western countries, often associated with neurological or endocrinological problems and where autism has been reported in severe … WebAniridia 1; Foveal hypoplasia 1; Coloboma of optic nerve; Autosomal dominant keratitis; Optic nerve hypoplasia, bilateral; Irido-corneo-trabecular dysgenesis; 11p partial monosomy syndrome; Congenital ocular coloboma; Annular epidermolytic ichthyosis; Arrhythmogenic right ventricular dysplasia 1; Rienhoff syndrome c言語 while文 do while 違い