ArticleJournal of clinical and diagnostic research : JCDR2014
Infantile onset alexander disease with normal head circumference: a genetically proven case report.
Article in Journal of clinical and diagnostic research : JCDR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 8 citations in OpenAlex.
- Heterogeneity of white matter astrocytes in the human brain.Acta neuropathologica · 2022Review
- Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia.Balkan journal of medical genetics : BJMG · 2019Article
- Infantile Alexander Disease: Case Report and Review of Literature.Journal of clinical and diagnostic research : JCDR · 2017Article
- Astrocyte heterogeneity in the brain: from development to disease.Frontiers in cellular neuroscience · 2015Review
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Alexander disease (AD) is an autosomal dominant leukodystrophy which predominantly affects infants and children. The infantile form comprises the most common form of AD. It presents before two years of age and characterized by macrocephaly, psychomotor regression, spasticity, pyramidal sign, ataxia and seizures. The diagnosis is based on magnetic resonance imaging (MRI) findings and confirmed by Glial fibrillary acidic protein (GFAP) gene molecular testing. We report an Indian case with normal head circumference.
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Registered trials
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