Diencephalic Syndrome: A Rare Entity with Its Anaesthetic Management and Post-operative Complications of Diabetes Insipidus and Thrombocytopenia
Russell first described the diencephalic syndrome in 1951. It is a rare syndrome and usually presents in children as a cause of failure to thrive despite normal, or even increased appetite, with preservation of linear growth. The treatment options vary from endoscopic biopsy followed by chemotherap...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
European Medical Journal
2022-08-01
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| Series: | European Medical Journal |
| Online Access: | https://emj.emg-health.com/flagship-journal/article/diencephalic-syndrome-a-rare-entity-with-its-anaesthetic-management-and-post-operative-complications-of-diabetes-insipidus-and-thrombocytopenia/ |
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