Classical Lissencephalies and Subcortical Band Heterotopias [klasické lisencefalie a subkortikální pruhovité heterotopie]
- Terms
- 
            komplex agyrie-pachygyrie-subkortikální pruhovítá heterotopie 
 lisencefalie 1. typu
 lisencefalie klasická
 lisencefalie Miller-Diekerova typu
 lisencefalie Millerova-Diekerova
 lisencefalie typ 1
 lisencefalie vázaná na chromozóm X
 Miller-Diekerova lissencephalie
 Miller-Diekerův syndrom
 subkortikální pruhovitá heterotopie
 syndrom delece chromozomu 17p13.3
 X-vázaná lisencefalie
 X-vázaná lisencefalie 1
- 
            Agyria-Pachygyria-Band Spectrum 
 Chromosome 17p13.3 Deletion Syndrome
 Classic Lissencephaly
 Classical Lissencephaly Syndrome
 Double Cortex Syndrome
 Heterotopia, Subcortical Band
 Isolated Lissencephaly Sequence
 Lissencephalies, Classical
 Lissencephaly 1
 Lissencephaly Sequence, Isolated
 Lissencephaly Syndrome, Miller-Dieker
 Lissencephaly Type 1
 Lissencephaly-Subcortical Band Heterotopia
 Lissencephaly, Classic
 Lissencephaly, Miller-Dieker
 Lissencephaly, Type 1
 Lissencephaly, X-Linked
 Lissencephaly, X-Linked, 1
 Miller-Dieker Lissencephaly Syndrome
 Miller-Dieker Syndrome
 Subcortical Band Heterotopia
 Subcortical Laminar Heterotopia
 Type 1 Lissencephaly
 X-Linked Lissencephaly
Disorders comprising a spectrum of brain malformations representing the paradigm of a diffuse neuronal migration disorder. They result in cognitive impairment; SEIZURES; and HYPOTONIA or spasticity. Mutations of two genes, LIS1, the gene for the non-catalytic subunit of PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE IB; and DCX or XLIS, the gene for doublecortin, have been identified as the most common causes of disorders in this spectrum. Additional variants of classical (Type I) lissencephaly have been linked to RELN, the gene for reelin, and ARX, the gene for aristaless related homeobox protein. (From Leventer, R.J., et al, Mol Med Today. 2000 Jul;6(7):277-84 and Barkovich, A.J., et al, Neurology. 2005 Dec 27;65(12):1873-87.)
- DUI
- D054221 MeSH Browser
- CUI
- M0501375
- Previous indexing
- Cerebral Cortex/abnormalities (1993-2007)
- History note
- 2008
- Public note
- 2008
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis 2
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 1
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 1
- UR
- urine
- VE
- veterinary
- VI
- virology
Band Heterotopia of Brain Disease MeSH Browser
Double cortex Disease MeSH Browser
Lissencephaly and agenesis of corpus callosum Disease MeSH Browser
Lissencephaly, X-Linked, 2 Disease MeSH Browser
Subcortical Band Heterotopia, X-Linked Disease MeSH Browser