Wiskott-Aldrich Syndrome [Wiskottův-Aldrichův syndrom]

topical
20
Terms

Aldrich Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
Imd2
Immunodeficiency 2
Wiskott Syndrome

Persistent link   https://www.medvik.cz/link/D014923
Definition

A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common.

DUI
D014923 MeSH Browser
CUI
M0022985
History note
85; was ALDRICH SYNDROME 1963-84
Online note
use WISKOTT-ALDRICH SYNDROME to search ALDRICH SYNDROME 1966-84
Public note
85; was ALDRICH SYNDROME 1963-84

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 4
DI
diagnosis 10
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 1
EH
ethnology
ET
etiology 2
GE
genetics 7
HI
history
IM
immunology 3
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 3
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 9
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 976
C15.378.100 Blood Coagulation Disorders 600
C15.378.100.100 Blood Coagulation Disorders, Inherited 64
C15.378.100.100.037 Activated Protein C Resistance 105
C15.378.100.100.056 Afibrinogenemia 39
C15.378.100.100.075 Antithrombin III Deficiency 24
C15.378.100.100.080 Bernard-Soulier Syndrome 9
C15.378.100.100.300 Factor V Deficiency 7
C15.378.100.100.310 Factor VII Deficiency 6
C15.378.100.100.320 Factor X Deficiency 2
C15.378.100.100.325 Factor XI Deficiency 12
C15.378.100.100.330 Factor XII Deficiency 8
C15.378.100.100.335 Factor XIII Deficiency 4
C15.378.100.100.500 Hemophilia A 691
C15.378.100.100.510 Hemophilia B 216
C15.378.100.100.515 Hermanski-Pudlak Syndrome 7
C15.378.100.100.550 Hypoprothrombinemias 4
C15.378.100.100.690 Protein C Deficiency 31
C15.378.100.100.820 Thrombasthenia 7
C15.378.100.100.900 von Willebrand Diseases 103
C15.378.100.100.970 Wiskott-Aldrich Syndrome 20
C15.378.243 Cytopenia 3
C15.378.243.750 Leukopenia 127
C15.378.243.750.605 Lymphopenia 45
C15.378.243.750.605.800 T-Lymphocytopenia, Idiopathic CD4-Positive
C15.378.243.750.605.900 Wiskott-Aldrich Syndrome 20
C15.378.463 Hemorrhagic Disorders 95
C15.378.463.067 Afibrinogenemia 39
C15.378.463.080 Bernard-Soulier Syndrome 9
C15.378.463.250 Disseminated Intravascular Coagulation 210
C15.378.463.300 Factor V Deficiency 7
C15.378.463.310 Factor VII Deficiency 6
C15.378.463.320 Factor X Deficiency 2
C15.378.463.325 Factor XI Deficiency 12
C15.378.463.330 Factor XII Deficiency 8
C15.378.463.335 Factor XIII Deficiency 4
C15.378.463.500 Hemophilia A 691
C15.378.463.510 Hemophilia B 216
C15.378.463.515 Hemostatic Disorders 49
C15.378.463.550 Hypoprothrombinemias 4
C15.378.463.735 Platelet Storage Pool Deficiency 1
C15.378.463.740 Purpura, Thrombocytopenic, Idiopathic 172
C15.378.463.810 Thrombasthenia 7
C15.378.463.825 Thrombocythemia, Essential 94
C15.378.463.841 Vitamin K Deficiency 42
C15.378.463.920 von Willebrand Diseases 103
C15.378.463.950 Waterhouse-Friderichsen Syndrome 11
C15.378.463.960 Wiskott-Aldrich Syndrome 20
C15.378.553 Leukocyte Disorders 18
C15.378.553.546 Leukopenia 127
C15.378.553.546.605 Lymphopenia 45
C15.378.553.546.605.800 T-Lymphocytopenia, Idiopathic CD4-Positive
C15.378.553.546.605.900 Wiskott-Aldrich Syndrome 20
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.099.037 Activated Protein C Resistance 105
C16.320.099.056 Afibrinogenemia 39
C16.320.099.075 Antithrombin III Deficiency 24
C16.320.099.080 Bernard-Soulier Syndrome 9
C16.320.099.300 Factor V Deficiency 7
C16.320.099.310 Factor VII Deficiency 6
C16.320.099.320 Factor X Deficiency 2
C16.320.099.325 Factor XI Deficiency 12
C16.320.099.330 Factor XII Deficiency 8
C16.320.099.335 Factor XIII Deficiency 4
C16.320.099.417 Gray Platelet Syndrome 1
C16.320.099.500 Hemophilia A 691
C16.320.099.510 Hemophilia B 216
C16.320.099.515 Hermanski-Pudlak Syndrome 7
C16.320.099.550 Hypoprothrombinemias 4
C16.320.099.690 Protein C Deficiency 31
C16.320.099.820 Thrombasthenia 7
C16.320.099.920 von Willebrand Diseases 103
C16.320.099.970 Wiskott-Aldrich Syndrome 20
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.322.030 Aicardi Syndrome
C16.320.322.061 Androgen-Insensitivity Syndrome 56
C16.320.322.068 Barth Syndrome 6
C16.320.322.076 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.322.092 Choroideremia 3
C16.320.322.100 Dent Disease 1
C16.320.322.108 Dyskeratosis Congenita 9
C16.320.322.116 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.322.124 Fabry Disease 189
C16.320.322.186 Focal Dermal Hypoplasia 6
C16.320.322.201 Glycogen Storage Disease Type IIb 11
C16.320.322.217 Glycogen Storage Disease Type VIII
C16.320.322.233 Granulomatous Disease, Chronic 54
C16.320.322.235 Hemophilia B 216
C16.320.322.237 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C16.320.322.241 Ichthyosis, X-Linked 9
C16.320.322.370 Isolated Noncompaction of the Ventricular Myocardium 11
C16.320.322.500 X-Linked Intellectual Disability 18
C16.320.322.562 Muscular Dystrophy, Duchenne 136
C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.322.750 Oculocerebrorenal Syndrome 9
C16.320.322.828 Ornithine Carbamoyltransferase Deficiency Disease 20
C16.320.322.906 Pelizaeus-Merzbacher Disease 11
C16.320.322.937 Wiskott-Aldrich Syndrome 20
C16.320.322.968 X-Linked Combined Immunodeficiency Diseases 4
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.798.250 Ataxia Telangiectasia 48
C16.320.798.313 Bloom Syndrome 11
C16.320.798.375 Chediak-Higashi Syndrome 4
C16.320.798.500 Hereditary Complement Deficiency Diseases 5
C16.320.798.625 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.798.688 Job Syndrome 16
C16.320.798.719 Leukocyte-Adhesion Deficiency Syndrome 3
C16.320.798.750 Severe Combined Immunodeficiency 64
C16.320.798.875 Wiskott-Aldrich Syndrome 20
C20 Immune System Diseases 748
C20.673 Immunologic Deficiency Syndromes 1 110
C20.673.627 Lymphopenia 45
C20.673.627.800 T-Lymphocytopenia, Idiopathic CD4-Positive
C20.673.627.900 Wiskott-Aldrich Syndrome 20
C20.673.795 Primary Immunodeficiency Diseases 48
C20.673.795.250 Ataxia Telangiectasia 48
C20.673.795.313 Bloom Syndrome 11
C20.673.795.375 Chediak-Higashi Syndrome 4
C20.673.795.500 Hereditary Complement Deficiency Diseases 5
C20.673.795.625 Hyper-IgM Immunodeficiency Syndrome 4
C20.673.795.688 Job Syndrome 16
C20.673.795.719 Leukocyte-Adhesion Deficiency Syndrome 3
C20.673.795.750 Severe Combined Immunodeficiency 64
C20.673.795.875 Wiskott-Aldrich Syndrome 20

Wiskott-Aldrich Syndrome, Autosomal Dominant Form Disease MeSH Browser

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