Immune thrombocytopenia in Kabuki syndrome, a comparison with non-Kabuki cases in the UK paediatric ITP registry
Our findings suggest that the clinical presentation and course of ITP in children with KS are comparable to those of general ITP patients. Despite the elevated risk of ITP in KS, the manifestations of the condition do not differ significantly.
Authors
- John D. Grainger (ORCID: https://orcid.org/0000-0003-2626-0647)
- Lianna Reynolds (ORCID: https://orcid.org/0000-0001-8079-0804)
- Benjamin David Williams (ORCID: https://orcid.org/0000-0002-3144-5390)
- Gerard Gurumurthy
Institutions
- Greater Manchester Mental Health NHS Foundation Trust (GB)
- University of Manchester (GB)
- Royal Manchester Children's Hospital (GB)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2025-05-26
- DOI
- https://doi.org/10.1186/s13023-025-03743-y
- Primary Topic
- Immunodeficiency and Autoimmune Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00