Case Report: Hemophagocytic Lymphohistiocytosis Prior to the Onset of Leukemia in a Boy With CDK13 -Related Disorder

Cardinal features of -related disorders are characterized by intellectual disability, developmental delay, dysmorphic facial features, structural heart defect and structural brain abnormality. A 9-year-old boy presented with intellectual disability, development delay, characteristic craniofacial fea...

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Veröffentlicht in:Frontiers in genetics 2022-05, Vol.13, p.858668
Hauptverfasser: Cui, Dongyan, Wang, Songmi, Zhang, Ai, Liu, Aiguo, Hu, Qun
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Sprache:eng
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Zusammenfassung:Cardinal features of -related disorders are characterized by intellectual disability, developmental delay, dysmorphic facial features, structural heart defect and structural brain abnormality. A 9-year-old boy presented with intellectual disability, development delay, characteristic craniofacial features, brain malformation, cryptorchidism, autism spectrum disorder, and recently, recurrent hemophagocytic lymphohistiocytosis (HLH) in a half year period. Further investigation revealed the diagnosis of -related disorder. Finally, we found the underlying cause of HLH is acute lymphoblastic leukemia. Probably leukemia was a coincidental finding in this boy with related disorder, but the case herein suggests that individuals with -related disorder also face risk of developing cancers. Further detailed information could enable us to clarify this presentation because of only limited investigation in affected cases.
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2022.858668