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Jacobsen Syndrome: A Case Report With Olfactory Bulb Agenesis, Severe Endocrinopathy, and Neurodevelopmental Delay
Sajjad Ghanim Al-Badri1, Aditya Duhan2, Rania H Al-Taie3
1College of Medicine, University of Baghdad Baghdad Iraq.
Clinical Case Reports
|October 13, 2025
Abstract:
Jacobsen syndrome is a rare 11q deletion disorder with multisystem involvement. This case highlights a complex unbalanced 11;15 translocation, olfactory bulb agenesis, extensive white matter abnormalities, and severe endocrinopathies, emphasizing the need for comprehensive genetic and neuroimaging evaluations.
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