Systemic Mastocytosis
What's New
Last Posted: Sep 03, 2024
- Mast cell disorders and Hymenoptera venom-triggered anaphylaxis: evaluation and management.
Nathan A Boggs, et al. The journal of allergy and clinical immunology. In practice 2024 0 - Utility of KIT Mutations in Myeloid Neoplasms Without Documented Systemic Mastocytosis to Detect Hidden Mast Cells in Bone Marrow.
Do Hwan Kim, et al. Clinical lymphoma, myeloma & leukemia 2024 0 - Prevalence and impact of the KIT M541L variant in patients with mastocytosis.
Luisa N Dominguez Aldama, et al. Oncotarget 2024 0 521-531 - Underlying systemic mastocytosis in patients with unexplained osteoporosis: score proposal.
Ilaria Tanasi, et al. Bone 2024 0 117141 - Standardized indolent systemic mastocytosis evaluations across a healthcare system: implications for screening accuracy.
Jeremy C McMurray, et al. Blood 2024 0 - A multi-center retrospective comparison between systemic mastocytosis with t(8;21) AML and KIT mutant t(8;21) AML.
Zhibo Zhang, et al. Blood advances 2024 0 - An elevated prevalence of hereditary alpha-tryptasemia in all mastocytosis subtypes: pathophysiological implications.
Laura Polivka, et al. The Journal of allergy and clinical immunology 2023 0 - Severe food allergy reactions are associated with ?-tryptase.
Abigail Lang, et al. The Journal of allergy and clinical immunology 2023 0 - Digital PCR: A Sensitive and Precise Method for KIT D816V Quantification in Mastocytosis.
Greiner Georg, et al. Clinical chemistry 2017 0 (3) 547-555 - Case Report: Unusual Manifestation of KIT Negative Systemic Mastocytosis.
Cáceres-Nazario Beatriz, et al. American journal of hematology/oncology 2017 0 (12) 24-27
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
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- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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