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- W4213058360 abstract "We would like to share ideas on “Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India.”[1] Prajapati et al noted that “Infantile onset with thalamic atrophy on MRI is common in CLN1 and refractory epilepsy, visual impairment, and specific EEG changes are common … diagnosis and genetic testing in subtyping. Thus, a multimode approach played a role in the diagnosis of NCL.”[1] We agree that observations in the present report might be clinically useful. Some clinical features might be more common in CLN1, whereas others are more common in CLN2. The observed patterns in a previous Indian report showed some differences.[2] Due to the few patients and since there is no statistical proof for difference, the observed clinical features might not be able to discriminate and might not “helpful in selecting enzyme assay for CLN1 versus CLN2.”" @default.
- W4213058360 created "2022-02-24" @default.
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- W4213058360 date "2022-02-21" @default.
- W4213058360 modified "2023-09-27" @default.
- W4213058360 title "Ceroid Lipofuscinosis in Children: Correspondence" @default.
- W4213058360 cites W3047298735 @default.
- W4213058360 cites W3125636514 @default.
- W4213058360 doi "https://doi.org/10.1055/s-0042-1743193" @default.
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