MeSH Browser

MeSH Heading: Aicardi Syndrome
Tree Number(s): C10.500.034.687; C11.270.019; C16.131.162; C16.131.666.034.687; C16.320.290.019; C16.320.322.030
Unique ID: D058540
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D058540
Scope Note: A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.
Entry Term(s): Agenesis of Corpus Callosum with Chorioretinal Abnormality; Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities; Aicardi's Syndrome; Callosal Agenesis and Ocular Abnormalities; Chorioretinal Anomalies with Acc; Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
Previous Indexing: Syndrome (1972-2010)
Public MeSH Note: 2011
History Note: 2011
Date Established: 2011/01/01
Date of Entry: 2010/06/25
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Aicardi Syndrome MeSH Descriptor Data 2024