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Being an uncommon condition and the lack of specific symptoms often result in a delayed diagnosis or even misdiagnosis, which, in addition to its progressive nature, can lead to dysfunction of vital organs, and ultimately, a poor prognosis. In this report, we present a unique case of GLA in an upper Egyptian female child. Increasing awareness of the possible phenotypic presentations of such anomalies can lead to early diagnosis and possibly more effective management before significant organ damage ensues.<\/jats:p>","DOI":"10.1111\/cup.14674","type":"journal-article","created":{"date-parts":[[2024,6,27]],"date-time":"2024-06-27T10:24:02Z","timestamp":1719483842000},"page":"746-750","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Generalized lymphatic anomaly: A case report and review of literature"],"prefix":"10.1111","volume":"51","author":[{"given":"Eman R. 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