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The clinical symptoms included microcephaly, brachygnathia, central and peripheral hypotonia, and developmental delay (non\u2010verbal), among others. On comparison with published literature, even patients with the same mutation present different clinical symptoms.<\/jats:p><\/jats:sec><jats:sec><jats:title>Abstract<\/jats:title><jats:p>This case report presents a child with PURA\u2010related neurodevelopmental disorder, caused by the heterozygous pathogenic variant c.175C&gt;T (p.Gln59*), whose symptoms included microcephaly, brachygnathia, the development of a high anterior hairline, hip dysplasia, strabismus, severe hypotonia, developmental delay (non\u2010meaningful verbal), feeding difficulties, and respiratory difficulties. His development ceased with age, such that his development at 10 years corresponded to an infant of 6 months. Moreover, even patients with the same variant can have different clinical symptoms, such as the presence or absence of epilepsy or congenital malformations. Therefore, we should follow his long\u2010term clinical course and provide medical support as necessary.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccr3.7779","type":"journal-article","created":{"date-parts":[[2023,9,7]],"date-time":"2023-09-07T05:44:58Z","timestamp":1694065498000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Heterozygous c.<scp>175C<\/scp>&gt;T variant in <i>PURA<\/i> gene causes severe developmental delay"],"prefix":"10.1002","volume":"11","author":[{"given":"Yusuke","family":"Noda","sequence":"first","affiliation":[{"name":"Department of Pediatrics Kumamoto University Hospital  Kumamoto Japan"},{"name":"Department of Pediatrics Graduate School of Medical Sciences Kumamoto University  Kumamoto 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