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It can present with pituitary hormone deficiencies, growth failure, visual impairment, and neurological symptoms. SOD can be diagnosed at different time points\u2014from the prenatal period to childhood. Our team cared for a baby girl who presented with recurrent hypoglycaemia, conjugated hyperbilirubinemia, and hormonal deficiencies, prompting investigations that resulted in an early diagnosis of SOD. This case report highlights the importance of considering neuroimaging to exclude septo\u2010optic dysplasia in term infants with recurrent hypoglycaemia, low cortisol, and growth hormone levels, as timely diagnosis with early hormone replacement reduces long\u2010term morbidities.<\/jats:p>","DOI":"10.1002\/ccr3.71985","type":"journal-article","created":{"date-parts":[[2026,2,10]],"date-time":"2026-02-10T04:40:13Z","timestamp":1770698413000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Recurrent Hypoglycaemia Leading to Early Diagnosis of Septo\u2010Optic Dysplasia in a Small\u2010for\u2010Gestational\u2010Age Infant\u2014A Case Report"],"prefix":"10.1002","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6656-4701","authenticated-orcid":false,"given":"Yuan Rui Leon","family":"Tan","sequence":"first","affiliation":[{"name":"Department of Neonatology KK Women's and Children's Hospital  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