Chronic Granulomatous Disease
Description
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency, mainly affecting phagocytes, which is characterized by an increased susceptibility to severe and recurrent bacterial and fungal infections, along with the development of granulomas.
Genes related to Chronic Granulomatous Disease
- NCF4
- CYBA
- NCF1
- NCF2
- CYBB
Clinical Features
Top most frequent phenotypes and symptoms related to Chronic Granulomatous Disease
- Hepatomegaly
- Fever
- Splenomegaly
- Recurrent respiratory infections
- Malabsorption
- Sepsis
- Otitis media
- Eczema
- Cutaneous photosensitivity
- Sinusitis
And another 12 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Based on the latest data available CHRONIC GRANULOMATOUS DISEASE have a estimated birth prevalence of 0.46 per 100k in Europe.— No data available about the known clinical features onset.
Alternative names
Chronic Granulomatous Disease Is also known as chronic septic granulomatosis, cgd.
Researches and researchers
Doctors, researchs, and experts related to Chronic Granulomatous Disease extracted from public data.
Chronic Granulomatous Disease Experts map
Current Researchs and researchers
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Responsible for diagnostic tests - Investigator of research project - Director of laboratory - Quality manager
GRENOBLE — Dr Marie José STASIA
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Institution/s:
— Département de Biochimie, Toxicologie et Pharmacologie, CHU de Grenoble et des Alpes - Institut de biologie et de pathologie -
Research area/topic::
USIDNET: modelization of X+CGD chronic granulomatous disease and Nox2 super oxidase mutants in the PLB-985 cell line to study the NADPH oxidase activation process
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Institution/s:
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Investigator of research project
GRENOBLE — Dr Marie-Hélène PACLET
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Institution/s:
— CHU de Grenoble site Nord - Hôpital Albert Michallon -
Research area/topic::
Validation of a new concept of cell therapy by transfer of proteins in enzymopathies: application to the Chronic septic granulomatosis
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Institution/s:
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Investigator of research project - Director of department
DRESDEN — Pr Angela RÖSEN-WOLFF
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Institution/s:
— Kinder- und Frauenzentrum, Universitätsklinikum Carl Gustav Carus an der TU Dresden -
Research area/topic::
Identification and characterization of phagocyte defects
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Institution/s:
-
Investigator of research project - Director of laboratory - Director of department
FRANKFURT AM MAIN — Pr Harald VON MELCHNER
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Institution/s:
— Klinikum der Johann Wolfgang Goethe-Universität Frankfurt -
Research area/topic::
Employing gene trapping for the correction of the Gp91phox (Nox2) mutation in chronic granulomatous disease (X-CGD)
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Institution/s:
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Responsible for diagnostic tests - Principal investigator of clinical trial - Investigator of research project - Coordinator of research network
MILANO — Pr Alessandro AIUTI
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Institution/s:
— Istituto San Raffaele Telethon per la Terapia Genica - TIGET -
Research area/topic::
Gene therapy for Chronic Granulomatous Disease
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Institution/s:
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Responsible for diagnostic tests - Investigator of research project
MILANO — Dr Barbara CASSANI
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Institution/s:
— Dipartimento dei Servizi Diagnostici, Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano -
Research area/topic::
X-linked Chronic Granulomatosis: molecular and cellular mechanisms underlying intestinal inflammation
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Institution/s:
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Investigator of research project
STOCKHOLM — Pr Bengt FADEEL
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Institution/s:
— Karolinska Institutet - Solna -
Research area/topic::
Programmed cell clearance: molecular mechanisms and role in pathogenesis and treatment of chronic inflammation
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Institution/s:
Chronic Granulomatous Disease Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
Chronic Granulomatous Disease - NCF4 Sequencing.
By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado (United States).
NCF4
Specificity
100 %
Genes
20 % |
Chronic granulomatous disease (sequence analysis of NCF4 gene).
By CGC Genetics (Portugal).
NCF4
Specificity
100 %
Genes
20 % |
Chronic Granulomatous Disease via NCF4 Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
NCF4
Specificity
100 %
Genes
20 % |
Chronic Granulomatous Disease Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
CYBA, CYBB, NCF2, NCF4
Specificity
100 %
Genes
80 % |
Chronic granulomatous disease panel.
By Centogene AG - the Rare Disease Company (Germany).
CYBA, CYBB, NCF1, NCF2, NCF4
Specificity
100 %
Genes
100 % |
Defects of phagocytosis Panel.
By CeGaT GmbH (Germany).
STAT1, TAZ, TCIRG1, TCN2, TERT, WAS, WIPF1, ACTB, VPS45, HPS3, HPS4, HAX1, HPS5, DTNBP1, CEBPE, HPS6, SBDS, SLC35C1, BLOC1S3, VPS13B , (...)
View the complete list with 39 more genes
Specificity
9 %
Genes
100 % |
Chronic granulomatous disease, autosomal recessive (CGD).
By Department of Clinical Immunology Odense University Hospital (Denmark).
CYBA, NCF1, NCF2, NCF4
Specificity
100 %
Genes
80 % |
Invitae Monogenic Autoimmunity Panel.
By Invitae (United States).
RMRP, SH2D1A, SLC7A7, BTK, STAT1, STAT3, STAT5B, STIM1, STX11, STXBP2, TBX1, FAS, CD27, TNFSF12, CD40LG, FASLG, TPP2, TREX1, ACP5, UNG , (...)
View the complete list with 53 more genes
Specificity
6 %
Genes
80 % |
You can get up to 61 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like RIPPLING MUSCLE DISEASE 2; RMD2 SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6 LEBER CONGENITAL AMAUROSIS 11; LCA11 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2
Chronic Granulomatous Disease - NCF4 Sequencing.
Chronic granulomatous disease (sequence analysis of NCF4 gene).
Chronic granulomatous disease, autosomal recessive (CGD).