Acute Promyelocytic Leukemia
Description
Acute promyelocytic leukemia (APL) is an aggressive form of acute myeloid leukemia (AML; see this term), characterized by arrest of leukocyte differentiation at the promyelocyte stage, due to a specific chromosomal translocation t(15;17) in myeloid cells. APL manifests with easy bruising, hemorrhagic diathesis and fatigue.
Genes related to Acute Promyelocytic Leukemia
- PRKAR1A
- NPM1
- PML
- FIP1L1
- NRAS
- FLT3
- ZBTB16
- IDH2
- NUMA1
- RAP1GAP
- FNDC3B
- STAT5B
- ITGAM
- DNMT3A
- IRF2BP2
- IDH1
- ASXL1
- F3
- ITGAL
- TET2
- IFNG
- GLI2
- WT1
- RARA
- THBD
- GLI1
- TBL1XR1
- SMO
- IL17A
- BIRC5
- KIT
- ITGAX
- ITGB2
- AKT1
- NABP1
- AQP9
Clinical Features
Phenotypes and symptoms related to Acute Promyelocytic Leukemia
- Leukemia
- Acute promyelocytic leukemia
- Abnormal granulocytopoietic cell morphology
Incidence and onset information
— Based on the latest data available ACUTE PROMYELOCYTIC LEUKEMIA have a estimated incidence of 0.11 per 100k worldwide.— No data available about the known clinical features onset.
Alternative names
Acute Promyelocytic Leukemia Is also known as acute myeloid leukemia with t(15;17)(q22;q12);(pml/raralpha) and variants, acute myeloblastic leukemia 3, apml, aml m3, aml with t(15;17)(q22;q12);(pml/raralpha) and variants, leukemia, acute promyelocytic.
Researches and researchers
Doctors, researchs, and experts related to Acute Promyelocytic Leukemia extracted from public data.
Acute Promyelocytic Leukemia Experts map
Current Researchs and researchers
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Responsible for diagnostic tests - Investigator of research project
LEUVEN — Pr Peter A VANDENBERGHE
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Institution/s:
— Department of Human Genetics, University Hospitals Leuven - Gasthuisberg -
Research area/topic::
The role of RAS- and RHO-GTPases, their regulators and mediators in the pathogenesis of myeloid malignancies.
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Institution/s:
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Coordinator of expert centre - Clinical expert - Principal investigator of clinical trial - Investigator of research project
DRESDEN — Pr Uwe PLATZBECKER
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Institution/s:
— Universitätsklinikum Carl Gustav Carus an der TU Dresden
— Universitätsklinikum Carl Gustav Carus an der TU Dresden -
Research area/topic::
NAPOLEON Registry of the German AML Intergroup - National acute promyelocytic leukemia observational study
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Institution/s:
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Coordinator of expert centre - Clinical expert - Principal investigator of clinical trial - Investigator of research project - Coordinator of research network
MANNHEIM — Dr Susanne SAUßELE
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Institution/s:
— III. Medizinische Universitäts-Klinik, Universitätsklinikum Mannheim
— Universitätsmedizin Mannheim -
Research area/topic::
Competence Network 'acute and chronic leukemias'
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Institution/s:
-
Investigator of research project
STUTTGART — Pr Jochen GREINER
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Institution/s:
— Diakonie-Klinikum Stuttgart -
Research area/topic::
AMLSG 18-12: Maintenance therapy with Histamine Dihydrochloride and Interleukin-2 in adult AML patients with measurable minimal residual disease - a Non-interventional Study
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Institution/s:
Acute Promyelocytic Leukemia Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
Hereditary Endocrine Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States).
SDHA, SDHB, SDHC, SDHD, TP53, VHL, CDC73, SDHAF2, TMEM127, MAX, MEN1, PRKAR1A, PTEN, RET
Specificity
8 %
Genes
3 % |
Comprehensive Hereditary Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States).
RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A , (...)
View the complete list with 39 more genes
Specificity
4 %
Genes
6 % |
Inherited Cancer Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
BLM, SDHB, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, TSC1, TSC2, VHL, XRCC2, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, BRIP1, SDHAF2, TMEM127 , (...)
View the complete list with 28 more genes
Specificity
3 %
Genes
3 % |
VistaSeq Hereditary Cancer Panel.
By Molecular Diagnostic Laboratory University of Alberta (Canada).
BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, CDH1, CDK4, CDKN2A, BRIP1, ABRAXAS1, PALB2, APC, SMAD4, MLH1, MSH2, MSH6, MUTYH, NBN, ATM , (...)
View the complete list with 6 more genes
Specificity
4 %
Genes
3 % |
Vistaseq Hereditary Cancer Panel Without BRCA.
By Molecular Diagnostic Laboratory University of Alberta (Canada).
BMPR1A, STK11, EPCAM, TP53, CDH1, CDK4, CDKN2A, BRIP1, ABRAXAS1, PALB2, APC, SMAD4, MLH1, MSH2, MSH6, MUTYH, NBN, ATM, PMS2, PRKAR1A , (...)
View the complete list with 4 more genes
Specificity
5 %
Genes
3 % |
VistaSeq Endrocrine Cancer Panel.
By Molecular Diagnostic Laboratory University of Alberta (Canada).
SDHB, SDHC, SDHD, TP53, VHL, CDC73, TMEM127, MAX, MEN1, NF1, PRKAR1A, PTEN, RET
Specificity
8 %
Genes
3 % |
Hypoparathyroidism Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
STX16, TBCE, TBX1, CASR, CHD7, FAM111A, CYP24A1, AIRE, GATA3, GCM2, GNA11, GNAS, HADHA, HADHB, PDE4D, PRKAR1A, PTH
Specificity
6 %
Genes
3 % |
Hypoparathyroidism sequencing panel.
By Genetic Services Laboratory University of Chicago (United States).
STX16, TBCE, TBX1, CASR, CDH7, FAM111A, CYP24A1, AIRE, GATA3, GCM2, GNA11, GNAS, HADHA, HADHB, PDE4D, PRKAR1A, PTH
Specificity
6 %
Genes
3 % |
You can get up to 812 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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Hereditary Endocrine Cancer Panel.
VistaSeq Hereditary Cancer Panel.