Search
Descriptor English: Wiskott-Aldrich Syndrome
Descriptor Spanish: Síndrome de Wiskott-Aldrich
Descriptor síndrome de Wiskott-Aldrich
Entry term(s) síndrome de Aldrich
Scope note: Síndrome de inmunodeficiencia ligado al cromosoma X poco frecuente que se caracteriza por ECZEMA, LINFOPENIA e infecciones piógenas recurrentes. Ocurre exclusivamente en varones jóvenes. Típicamente, los valores de INMUNOGLOBULINA M son bajos y están elevados los de INMUNOGLOBULINA A e INMUNOGLOBULINA E. Son frecuentes las neoplasias malignas linforeticulares.
Descriptor Portuguese: Síndrome de Wiskott-Aldrich
Descriptor French: Syndrome de Wiskott-Aldrich
Entry term(s): Aldrich Syndrome
Eczema Thrombocytopenia Immunodeficiency Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndromes
Imd2
Immunodeficiency 2
Immunodeficiency 2s
Wiskott Aldrich Syndrome
Wiskott Syndrome
Wiskott Syndromes
Tree number(s): C15.378.100.100.970
C15.378.463.960
C15.378.553.546.605.900
C16.320.099.970
C16.320.322.937
C16.320.798.875
C20.673.627.900
C20.673.795.875
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D014923
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 85; was ALDRICH SYNDROME 1963-84
Online Note: use WISKOTT-ALDRICH SYNDROME to search ALDRICH SYNDROME 1966-84
History Note: 85; was ALDRICH SYNDROME 1963-84
DeCS ID: 15323
Unique ID: D014923
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1985/01/01
Date of Entry: 1999/01/01
Revision Date: 2015/06/23
Wiskott-Aldrich Syndrome - Preferred
Concept UI M0022985
Scope note 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.
Preferred term Wiskott-Aldrich Syndrome
Entry term(s) Aldrich Syndrome
Eczema Thrombocytopenia Immunodeficiency Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndromes
Imd2
Immunodeficiency 2
Immunodeficiency 2s
Wiskott Aldrich Syndrome
Wiskott Syndrome
Wiskott Syndromes



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey