Nasopharyngeal Carcinoma
Description
Nasopharyngeal carcinoma (NPC) is a tumor arising from the epithelial cells that cover the surface and line the nasopharynx.
Clinical Features
Phenotypes and symptoms related to Nasopharyngeal Carcinoma
- Neoplasm
 - Carcinoma
 - Neoplasia of the nasopharynx
 
Incidence and onset information
— Based on the latest data available NASOPHARYNGEAL CARCINOMA have a estimated prevalence of 2 per 100k worldwide.— No data available about the known clinical features onset.
Alternative names
Nasopharyngeal Carcinoma Is also known as npca, squamous cell carcinoma of the nasopharynx, npc, nasopharyngeal cancer.
Researches and researchers
Doctors, researchs, and experts related to Nasopharyngeal Carcinoma extracted from public data.
Nasopharyngeal Carcinoma Experts map
Current Researchs and researchers
- 
Investigator of research project
 AACHEN — Dr Sabrina FRANZEN 
- 
Institution/s:
— Klinik für Kinder- und Jugendmedizin, Universitätsklinikum Aachen - 
Research area/topic::
NPC-2014-GOPH-Registry: Multicenter registry for the treatment of nasopharyngeal carcinoma in Children and adolescent
 
 - 
Institution/s:
 
Nasopharyngeal Carcinoma Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	NFKBIA Sequencing.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). 
NFKBIA
 
Specificity
 
100 % 
Genes
 
50 %  | 
 	NFKBIA Deletion/duplication analysis.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). 
NFKBIA
 
Specificity
 
100 % 
Genes
 
50 %  | 
 	Primary Antibody Deficiency Panel, Sequencing and Deletion/Duplication.
By ARUP Laboratories, Molecular Genetics and Genomics (United States). 
SH2D1A, BTK, CD40, CD40LG, UNG, VAV1, AICDA, BLNK, CD19, CD79A, CD79B, CD81, LRBA, TNFRSF13C, TNFRSF13B, ADA, LRRC8A, CR2, ICOS, IGHM	, (...)
 
View the complete list with 15 more genes 
Specificity
 
3 % 
Genes
 
50 %  | 
 	Hypohidrotic ectodermal dysplasia with immunodeficiency (sequence analysis of NFKBIA gene).
By CGC Genetics (Portugal). 
NFKBIA
 
Specificity
 
100 % 
Genes
 
50 %  | 
 	Hyper IgM Syndrome Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States). 
SH2D1A, BTK, CD40, CD40LG, UNG, AICDA, MRE11, NBN, NFKBIA, ATM, PIK3CD
 
Specificity
 
10 % 
Genes
 
50 %  | 
 	IKBa Gene.
By Immunology Diagnostics Laboratory Seattle Children's Research Institute (United States). 
NFKBIA
 
Specificity
 
100 % 
Genes
 
50 %  | 
 	Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel.
By CeGaT GmbH (Germany). 
BCS1L, SNRPE, SOX18, ST14, TRPS1, IFT122, WNT10A, EDARADD, SHOC2, LPAR6, APCDD1, TP63, MPLKIP, UBR1, BANF1, CDH3, PORCN, CDSN, KCTD1, WDR19	, (...)
 
View the complete list with 35 more genes 
Specificity
 
2 % 
Genes
 
50 %  | 
 	Defects in innate immunity Panel.
By CeGaT GmbH (Germany). 
STAT1, TBK1, TLR3, TRAF3, TRAF3IP2, UNC93B1, CARD9, IL17F, TIRAP, IRAK4, TMC6, TICAM1, TMC8, CXCR4, IL17RA, APOL1, MCM4, MYD88, NFKBIA
 
Specificity
 
6 % 
Genes
 
50 %  | 
You can get up to 437 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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	NFKBIA Sequencing.
	Hypohidrotic ectodermal dysplasia with immunodeficiency (sequence analysis of NFKBIA gene).