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Paediatric surgical pathology - Level 5 - case 5
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Reference
Scheimberg I, Hoeger PH, Harper JI, Lake B, Malone M. Omenn's syndrome: differential diagnosis in infants with erythroderma and immunodeficiency. Pediatr Dev Pathol. 2001 May-Jun;4(3):237-45. doi: 10.1007/s100240010171. PMID: 11370261.
Elnour, Ibtisam B et al. “Omenn's Syndrome: A rare primary immunodeficiency disorder.”Sultan Qaboos University medical journalvol. 7,2 (2007): 133-8.
| Contributed by: | Pathology Portal |
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| Licence: | © All rights reserved More information on licences |
| Last updated: | 02 October 2023 |
| First contributed: | 04 September 2023 |
| Audience access level: | Full user |
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