Search references for PRIMARY IMMUNODEFICIENCY. Phrases containing PRIMARY IMMUNODEFICIENCY
See searches and references containing PRIMARY IMMUNODEFICIENCY!PRIMARY IMMUNODEFICIENCY
Resulting from inborn deficiencies in immune system
system is missing or does not function normally. To be considered a primary immunodeficiency (PID), the immune deficiency must be inborn, not caused by secondary
Primary_immunodeficiency
Lack of or compromised immune system
intrinsic defects in their immune system, or primary immunodeficiency. A person who has an immunodeficiency of any kind is said to be immunocompromised
Immunodeficiency
2 deficiency Immunodeficiency with multiple intestinal atresias (TTC7A deficiency) Hepatic venoocclusive disease with immunodeficiency (VODI) Vici syndrome
List of primary immunodeficiencies
List_of_primary_immunodeficiencies
Genetic disorder leading to severe impairment of the immune system
functional T cells and B cells. SCIDs are the most severe form of primary immunodeficiency, making their sufferers extremely vulnerable to infection due to
Severe combined immunodeficiency
Severe_combined_immunodeficiency
Immune disorder
Common variable immunodeficiency (CVID) is an inborn immune disorder characterized by recurrent infections and low antibody levels, specifically in immunoglobulin
Common variable immunodeficiency
Common_variable_immunodeficiency
Organisation for Primary Immunodeficiencies (IPOPI) is a global non-profit association for patients with primary immunodeficiencies (PIDs). Established
International Patient Organisation for Primary Immunodeficiencies
International_Patient_Organisation_for_Primary_Immunodeficiencies
Medical condition
Societies, more than 150 primary immunodeficiency diseases (PIDs) have been characterized. However, the number of acquired immunodeficiencies exceeds the number
Immune_disorder
Excess number of eosinophil cells in the blood
production of IL-3, leading to blood and tissue eosinophilia. Primary immunodeficiency diseases are inborn errors in the immune system due to defective
Eosinophilia
Human disease
Hypogammaglobulinemia can be caused by either a primary or secondary immunodeficiency. Primary immunodeficiencies are caused by a mutation or series of mutations
Hypogammaglobulinemia
European medical association
researchers who deal with primary immunodeficiency diseases (PID). The European Society for Primary Immunodeficiencies was founded first as an informal
European Society for Primary Immunodeficiencies
European_Society_for_Primary_Immunodeficiencies
Spectrum of conditions caused by HIV infection
The human immunodeficiency virus (HIV) is a retrovirus that attacks the immune system. Without treatment, it can lead to a spectrum of conditions including
HIV/AIDS
Medical treatment
immunoglobulin) to treat several health conditions. These conditions include primary immunodeficiency, immune thrombocytopenic purpura, chronic inflammatory demyelinating
Immunoglobulin_therapy
Medical condition
X-linked severe combined immunodeficiency (X-SCID) is an immunodeficiency disorder in which the body produces very few T cells and NK cells. In the absence
X-linked severe combined immunodeficiency
X-linked_severe_combined_immunodeficiency
American physician
in New York City. a specialist in primary immunodeficiency disorders. She is also director of the Immunodeficiency Clinic at Mount Sinai Hospital, and
Charlotte_Cunningham-Rundles
Puerto Rican VTuber and singer
research and improving the quality of life of people suffering from primary immunodeficiency. According to StreamsCharts, Ironmouse was the second most-watched
Ironmouse
Medical condition
hormonal immunodeficiencies consisting of 66 defective genes causing 58 different diseases. These diseases include severe combined immunodeficiency diseases
Inborn_errors_of_immunity
Medical condition
conditions which cause impairment of humoral immunity, which can lead to immunodeficiency. It can be mediated by insufficient number or function of B cells,
Humoral_immune_deficiency
Rare type of immunodeficiency disease
Essential Modulator (NEMO) deficiency syndrome is a rare type of primary immunodeficiency disease that has a highly variable set of symptoms and prognoses
NEMO_deficiency_syndrome
Human retrovirus, cause of AIDS
Human immunodeficiency viruses (HIVs) are two species of Lentivirus (a subgroup of retrovirus) that infect humans. Over time, they cause acquired immunodeficiency
HIV
Chromosomal anomaly
infancy 49,XXXXY may also be associated with increased rates of primary immunodeficiency. Much like Down syndrome, the mental effects of 49,XXXXY syndrome
XXXXY_syndrome
Iranian scientist
for his research in Primary Immunodeficiencies, characterization and treatment. He initiated the Iranian Primary Immunodeficiency Diseases Registry (IPIDR)
Nima_Rezaei
Iranian scientist
locator of National primary immunodeficiency Resource center. Member of European Society for Primary Immunodeficiencies (ESID). Editorial Board of [acta
Asghar_Aghamohammadi
Type of inflammatory bowel disease
The exact underlying immune problem is not clear, though it may be immunodeficiency. About half of the overall risk is related to genetics, with more than
Crohn's_disease
Medical condition
cells, which produce antibodies. First described in 1952, it is a primary immunodeficiency caused by a mutation on X chromosome (Xq21.3-q22), making it X-linked
X-linked_agammaglobulinemia
psychiatric symptoms in pediatric oncology, pediatric HIV and other primary immunodeficiencies. Pao was born to Pearl and Ping-Nie Pao. She is from Bethesda
Maryland_Pao
Medical condition
4th or 5th decade of life. The immunodeficiency may occur before or after the diagnosis of a thymoma. Immunodeficiency involves both deficient humoral
Thymoma_with_immunodeficiency
Medical condition
mycobacterial disease (MSMD) is a rare genetic disease. It is a primary immunodeficiency featured by molecular defects in IL12/IFNγ dependent signalling
Mendelian susceptibility to mycobacterial disease
Mendelian_susceptibility_to_mycobacterial_disease
Medical condition
cause life-threatening bacterial infections in children due to primary immunodeficiency. The infections can include pneumococal sepsis and meningitis.
Isolated_congenital_asplenia
Primary immune deficiency disorders
with primary immunodeficiency disorders (PIDs). X-linked agammaglobulinemia Common variable immunodeficiency (CVID) "X-linked Immunodeficiency With Hyper
Hyper_IgM_syndrome
Class of enzymes
for the treatment of primary immunodeficiency in adults. This includes, but is not limited to, common variable immunodeficiency, X-linked agammaglobulinemia
Hyaluronidase
its immunopathogenesis section since 2000. Holland researches primary immunodeficiencies and the genetic basis of susceptibility to infections. Holland
Steven_M._Holland_(physician)
International umbrella organization for immunology societies
(October 2007). "Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification
International Union of Immunological Societies
International_Union_of_Immunological_Societies
Medical condition
circumflexa. Netherton syndrome has recently been characterised as a primary immunodeficiency, which straddles the innate and acquired immune system, somewhat
Netherton_syndrome
Form of immune disorder
deficiencies are also an integral component of other well-known primary immunodeficiency diseases, such as Wiskott–Aldrich syndrome and ataxia–telangiectasia
IgG_deficiency
Preparation for acquired immunity to disease
immune status, age, health and nutritional status. One type of primary immunodeficiency disorder resulting in genetic failure is X-linked agammaglobulinemia
Vaccine
Medical condition
deficiency is a rare autosomal recessive disease characterized as a primary immunodeficiency syndrome. This disease was first identified within a white Mennonite
P14_deficiency
Medical condition
Uzel G, Matthews H, Lenardo MJ (April 2014). "XMEN disease: a new primary immunodeficiency affecting Mg2+ regulation of immunity against Epstein-Barr virus"
XMEN_disease
Medical school in Kerala, India
for Primary Immunodeficiency Disorders. This collaborative centre provides clinical care as well as genetic diagnosis for patients with primary immunodeficiency
Government Medical College, Kozhikode
Government_Medical_College,_Kozhikode
Species of virus
Feline immunodeficiency virus (FIV) is a lentivirus that affects cats worldwide with 2.5% to 4.4% of felines being infected. FIV was first isolated in
Feline_immunodeficiency_virus
Topics referred to by the same term
(Virus-Serum-Toxin Act), a U.S. federal law Virus-specific T-lymphocyte; see Primary immunodeficiency Search for "vst" , "v-st", "vs-t", or "v-s-t" on Wikipedia. All
VST
Mutation that shifts codon alignment
mutations is rare. Research into this is ongoing. One example is a primary immunodeficiency (PID), an inherited condition which can lead to an increase in
Frameshift_mutation
Plasmapheresis company based in Florida
medicine. Specific therapies include those treating hemophilia, primary immunodeficiency, von Willebrand disease, hereditary angioedema, hereditary respiratory
CSL_Plasma
Medical condition
short-limbed dwarfism due to skeletal dysplasia, variable level of immunodeficiency, and predisposition to cancer. It was first reported by Victor McKusick
Cartilage–hair_hypoplasia
Immunologist, pediatrician and professor
Pediatric Board. Ochs' research focuses on the molecular basis of primary immunodeficiency diseases with special interest in the genes that have been linked
Hans_D._Ochs
Immune disorder in the blood leading to hyperinflammation
arthritis. Secondary HLH also occurs rarely in immunodeficiency disorders such as severe combined immunodeficiency, DiGeorge syndrome, Wiskott–Aldrich syndrome
Hemophagocytic lymphohistiocytosis
Hemophagocytic_lymphohistiocytosis
Medical condition
Activated PI3K delta syndrome (APDS) is a primary immunodeficiency disease caused by activating gain of function mutations in the PIK3CD gene. The signs
Activated_PI3K_delta_syndrome
American lawyer
on the board of directors of the Jeffrey Modell Foundation for Primary Immunodeficiency Research and serves on the Advisory Board of Jane Doe No More,
Lisa_Wexler
Topics referred to by the same term
body mass index) Propidium iodide, a chemical used as a DNA stain Primary immunodeficiency Protease inhibitor (pharmacology), class of drugs used to treat
PI
Medical condition
Ankmalika (2017-09-05). "Selective IgM Deficiency—An Underestimated Primary Immunodeficiency". Frontiers in Immunology. 8. Frontiers Media SA. doi:10.3389/fimmu
Isolated primary immunoglobulin M deficiency
Isolated_primary_immunoglobulin_M_deficiency
Long-term inflammatory disease of the airways of the lungs
congenital conditions (cystic fibrosis, primary immunodeficiency, congenital heart disease, bronchopulmonary dysplasia, primary ciliary dyskinesia syndrome, tracheal
Asthma
Eosinophilic esophagitis Gastritis POEMS syndrome Raynaud's phenomenon Primary immunodeficiency Pyoderma gangrenosum At this time, there is not sufficient evidence
List_of_autoimmune_diseases
Immune response against an organism's own healthy cells
Familial hemophagocytic lymphohistiocytosis, an autosomal recessive primary immunodeficiency, is another example. Pancytopenia, rashes, swollen lymph nodes
Autoimmunity
Possession of multiple genetic lineages within a multi-cellular organism
"Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases". Journal of Allergy and Clinical Immunology. 143 (1):
Mosaic_(genetics)
Protein-coding gene in humans
Casanova JL, Etzioni A, Giliani S, Hammarström L, et al. (2001). "4 Primary immunodeficiency mutation databases". Advances in Genetics. Vol. 43. pp. 103–88
Common_gamma_chain
Branch of medicine that deals with immune responses associated with disease
are Primary Immunodeficiency, where the immune system is either missing a key component or does not function properly, and Secondary Immunodeficiency, where
Immunopathology
Human chromosome
Peripheral neuropathy Phosphofructokinase deficiency Primary ciliary dyskinesia Primary immunodeficiency Primitive neuroectodermal tumor Prostate cancer Romano–Ward
Chromosome_21
Medical condition
Neutrophil immunodeficiency syndrome is a condition caused by mutations in the Rac2 gene. It is a primary immunodeficiency by neutrophilia with severe
Neutrophil immunodeficiency syndrome
Neutrophil_immunodeficiency_syndrome
Permanent enlargement of the lung airways
localized to the lungs or systemic throughout the body. In these states of immunodeficiency, there is a weakened or absent immune system response to severe infections
Bronchiectasis
Excess amounts of gamma globulin in the blood
Mendelian Inheritance in Man (OMIM): Immunodeficiency with hyper IgM - 308230 Park LC X-linked Immunodeficiency with hyper IgM at eMedicine Lichtman,
Hypergammaglobulinemia
American paediatrician and immunologist
immunology fellowship in 1959. He and Janeway pioneered the study of primary immunodeficiency diseases at Boston Children's Hospital. Rosen discovered, early
Fred_Rosen_(physician)
Vaccine that uses a weakened form of the germ
Sobh, Ali; Bonilla, Francisco A. (November 2016). "Vaccination in Primary Immunodeficiency Disorders". The Journal of Allergy and Clinical Immunology: In
Attenuated_vaccine
Species of retrovirus
Simian immunodeficiency virus (SIV) is a species of retrovirus that cause persistent infections in at least 45 species of non-human primates. Based on
Simian_immunodeficiency_virus
Medical condition
Complement deficiency is an immunodeficiency of absent or suboptimal functioning of one of the complement system proteins. Because of redundancies in the
Complement_deficiency
Medical condition
thrombocytopenia). It is also sometimes called the eczema-thrombocytopenia-immunodeficiency syndrome in keeping with Aldrich's original description in 1954. The
Wiskott–Aldrich_syndrome
Autoimmune disease in which the immune system attacks healthy tissue
(April 2023). "Contribution of genetic variants associated with primary immunodeficiencies to childhood-onset systemic lupus erythematous". The Journal of
Lupus
Immunological test
HIV tests are used to detect the presence of the human immunodeficiency virus (HIV), the virus that can lead to AIDS, in serum, saliva, or urine. Such
Diagnosis_of_HIV/AIDS
Medical condition
nervous system (DLBCL-CNS), is a primary intracranial tumor appearing mostly in patients with severe immunodeficiency (typically patients with AIDS). It
Primary central nervous system lymphoma
Primary_central_nervous_system_lymphoma
German doctor and polymath (1821–1902)
doi:10.1309/LM3GYQTY79CPYLBI. Etzioni, Amos; Ochs, Hans D. (2014). Primary Immunodeficiency Disorders: A Historic and Scientific Perspective. Oxford: Elsevier
Rudolf_Virchow
Sri Lankan medical doctor
Free Hospital and University College London which is the largest Primary Immunodeficiency Centre in Europe. Seneviratne was a Consultant and Lead Clinician
Suranjith_Seneviratne
Medical condition
Lortholary, O. (August 14, 2014). "Prevention of Infections During Primary Immunodeficiency". Clinical Infectious Diseases. 59 (10). Oxford University Press
Combined_immunodeficiencies
Biomarker for B cell lineage
severe immunodeficiency syndromes characterized by diminished antibody production. Additionally, mutations in CD21 and CD81 can also underlie primary immunodeficiency
CD19
Medical condition
lymphoproliferations of the skin in individuals with primary immunodeficiency (i.e., individuals born with an immunodeficiency due to genetic causes), which had been
Primary cutaneous acral CD8 positive T cell lymphoproliferative disorder
Primary_cutaneous_acral_CD8_positive_T_cell_lymphoproliferative_disorder
Kinase that plays a role in B cell development
B-cell signalling. Mutations in the BTK gene are implicated in the primary immunodeficiency disease X-linked agammaglobulinemia (Bruton's agammaglobulinemia);
Bruton's_tyrosine_kinase
AIDS is caused by a human immunodeficiency virus (HIV), which originated in non-human primates in Central and West Africa. While various sub-groups of
History_of_HIV/AIDS
Absence of an organ or tissue from birth
the VACTERL syndrome.[citation needed] Thymic aplasia is a rare primary immunodeficiency with autosomal or X-linked recessive inheritance, characterized
Aplasia
Medical condition
Selective immunoglobulin A (IgA) deficiency (SIgAD) is a kind of immunodeficiency, a type of hypogammaglobulinemia. People with this deficiency lack immunoglobulin
Selective immunoglobulin A deficiency
Selective_immunoglobulin_A_deficiency
Infection spread in hospitals or health care facilities
Impaired immunity due to diseases such as haematological malignancy, primary immunodeficiency, HIV/AIDS or critical illness, including severe COVID-19 Presence
Hospital-acquired_infection
Australian biotechnology company
sub-cutaneous human immune globulin indicated for the treatment of primary immunodeficiency. This product gained FDA approval in January 2006. Von Willebrand
CSL_Limited
Gene therapy for Wiskott-Aldrich Syndrome
(GSK-2696275) is a gene therapy for Wiskott–Aldrich syndrome, a rare primary immunodeficiency caused by mutations in the gene that codes for Wiskott–Aldrich
OTL-103
Group of disorders
Still's disease, and rheumatoid arthritis; immunodeficiency disorders such as severe combined immunodeficiency, DiGeorge syndrome, Wiskott–Aldrich syndrome
Epstein–Barr virus–associated lymphoproliferative diseases
Epstein–Barr_virus–associated_lymphoproliferative_diseases
Hierarchical outline list of articles related to genetics
artificial chromosome (HAC) Human Genome Project human immunodeficiency virus (HIV) acquired immunodeficiency syndrome (AIDS) hybridization immunotherapy in situ
Outline_of_genetics
Medical condition
Warm antibody autoimmune hemolytic anemia Idiopathic Linked with primary immunodeficiency/immunodysregulation syndrome. Lymphoma or chronic lymphocytic leukemia
Acquired_hemolytic_anemia
Sexually transmitted infection
the millennium in many countries, often in combination with human immunodeficiency virus (HIV). This is believed to be partly due to unsafe drug use,
Syphilis
Medical condition
exhibited by those with Job Syndrome. Autosomal recessive: DOCK8 - DOCK8 Immunodeficiency Syndrome (DIDS) presents primarily with immune effects including HEIS
Hyperimmunoglobulin E syndrome
Hyperimmunoglobulin_E_syndrome
Medical condition
complement deficiencies only comprise approximately 2% of all primary immunodeficiency disorders. While the frequency of properdin deficiency has not
Properdin_deficiency
differentiation primary response gene 88 (MyD88) deficiency is a disorder of the innate immune system. It belongs to rare primary immunodeficiency characterized
Innate_immune_defect
US term for medical professional providing first-line care
Dodge W, Wagner E (1996). "Physicians' experience with the acquired immunodeficiency syndrome as a factor in patients' survival". N Engl J Med. 334 (11):
Primary_care_physician
Interleukin
interleukin-12/23-interferon gamma axis". In Ochs HD, Smith CI, Puck J (eds.). Primary immunodeficiency diseases : a molecular and genetic approach. New York: Oxford University
Interleukin_12
Medical condition
leukocyte adhesion defects. In: Ochs HD, Smith CIE, Puck JM, eds. Primary immunodeficiency diseases: a molecular and genetic approach. Oxford: Oxford University
Leukocyte adhesion deficiency-1
Leukocyte_adhesion_deficiency-1
Academy of Allergy and Clinical Immunology, European Society for Primary Immunodeficiencies, and World Allergy Organization. "FOCIS - Interdisciplinary Approaches
Federation of Clinical Immunology Societies
Federation_of_Clinical_Immunology_Societies
Sex-specific patterns of inheritance
degeneration of muscle cells. X-linked agammaglobulinemia is a primary immunodeficiency disorder that impairs the body's ability to produce antibodies
Sex_linkage
Infectious disease
risk factor globally for developing active TB is concurrent human immunodeficiency virus (HIV) infection; in 2023, 6.1% of those becoming infected with
Tuberculosis
Inc., Newburyport, MA (1970). Wertelecki, W., Peterson, R.D.A.: Primary Immunodeficiency Syndromes. In: Surgical Immunology. Ed., Munster, A.M., Grune Publishers
Wladimir_Wertelecki
Medical condition
Maleewan; Cooper, Megan A. (2020-01-01), "Chapter 28 - Autoimmunity in Primary Immunodeficiency Disorders", in Rose, Noel R.; Mackay, Ian R. (eds.), The Autoimmune
IPEX_syndrome
Condition negatively affecting an organism
one may look at the syndrome of acquired immunodeficiency (AIDS) or the causal agents: human immunodeficiency viruses (HIVs). In many cases, terms such
Disease
Measurement of genetic variations
Ferrante A (December 2006). "Molecular approaches in the diagnosis of primary immunodeficiency diseases". Human Mutation. 27 (12): 1163–1173. doi:10.1002/humu
SNP_genotyping
Branch of medicine studying the immune system
an immunodeficiency characterized by the suppression of CD4+ ("helper") T cells, dendritic cells and macrophages by the human immunodeficiency virus
Immunology
Enzyme and coding gene in humans
been associated with hyperimmunoglobulin E syndrome (HIES), a primary immunodeficiency characterized by elevated serum immunoglobulin E. The P1104A allele
Tyrosine_kinase_2
Rare metabolic disease
Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report". Journal of Korean Medical Science. 38
Combined malonic and methylmalonic aciduria
Combined_malonic_and_methylmalonic_aciduria
Indian academic research organization
Proteome Database Pancreatic Cancer Database Resource of Asian Primary Immunodeficiency Diseases IOB receives grants and fundings from various national
Institute of Bioinformatics, Bengaluru
Institute_of_Bioinformatics,_Bengaluru
travel, tourism, insurance
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
PRIMARY IMMUNODEFICIENCY
travel, tourism, insurance