serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.500 Nervous System Malformations .
C10.500.507 Malformations of Cortical Development .
C10.500.507.450 Malformations of Cortical Development, Group II .
C10.500.507.450.230 Classical Lissencephalies and Subcortical Band Heterotopias .
C10.500.507.450.499 Lissencephaly .
C10.500.507.450.499.230 Classical Lissencephalies and Subcortical Band Heterotopias .
C10.500.507.450.499.249 Cobblestone Lissencephaly .
C10.500.507.450.499.249.500 Walker-Warburg Syndrome .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.881 Walker-Warburg Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.507 Malformations of Cortical Development .
C16.131.666.507.450 Malformations of Cortical Development, Group II .
C16.131.666.507.450.230 Classical Lissencephalies and Subcortical Band Heterotopias .
C16.131.666.507.450.499 Lissencephaly .
C16.131.666.507.450.499.230 Classical Lissencephalies and Subcortical Band Heterotopias .
C16.131.666.507.450.499.249 Cobblestone Lissencephaly .
C16.131.666.507.450.499.249.500 Walker-Warburg Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.186 Classical Lissencephalies and Subcortical Band Heterotopias .
C16.320.577 Muscular Dystrophies .
C16.320.577.750 Walker-Warburg Syndrome .
D02 Organic Chemicals .
D02.455 Hydrocarbons .
D02.455.426 Hydrocarbons, Cyclic .
D02.455.426.559 Hydrocarbons, Aromatic .
D02.455.426.559.389 Benzene Derivatives .
D02.455.426.559.389.115 Benzhydryl Compounds .
D02.455.426.559.389.115.475 Meclizine .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.606 Piperazines .
D03.383.606.650 Meclizine .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Meclizine .
Agyrax .
Antivert .
Bonamine .
Bonine .
Chiclida .
D-Vert .
Meclizine Dihydrochloride .
Meclizine Hydrochloride .
Meclizine Monohydrochloride .
Ru-Vert-M .
D Vert .
DVert .
Dihydrochloride, Meclizine .
Hydrochloride, Meclizine .
Monohydrochloride, Meclizine .
Ru Vert M .
Histametizyn .
Meclozine .
Parachloramine .
A histamine H1 antagonist used in the treatment of motion sickness, vertigo, and nausea during pregnancy and radiation sickness. .
1.00
5153
 
Lissencephaly .
Broad Gyri of Cerebrum .
Large Gyri of Cerebrum .
Lissencephalia .
Macrogyria .
Agyrias .
Lissencephalies .
Macrogyrias .
Pachygyrias .
Agyria .
Pachygyria .
A smooth brain malformation of the CEREBRAL CORTEX resulting from the abnormal location of developing neurons during corticogenesis. It is characterized by an absence of normal convoluted indentations on the surface of the brain (agyria), or fewer and shallower indentations (pachygryia). There is a reduced number of cortical layers, typically 4 instead of 6, resulting in a thickened cortex, and reduced cerebral white matter that is a reversal of the normal ratio of cerebral white matter to cortex. .
0.80
5172
 
Classical Lissencephalies and Subcortical Band Heterotopias .
Agyria-Pachygyria-Band Spectrum .
Chromosome 17p13.3 Deletion Syndrome .
Classic Lissencephaly .
Classical Lissencephaly Syndrome .
Double Cortex Syndrome .
Isolated Lissencephaly Sequence .
Lissencephaly 1 .
Lissencephaly Sequence, Isolated .
Lissencephaly Syndrome, Miller-Dieker .
Lissencephaly Type 1 .
Lissencephaly, Classic .
Lissencephaly, Miller-Dieker .
Lissencephaly, X-Linked, 1 .
Miller-Dieker Lissencephaly Syndrome .
Subcortical Laminar Heterotopia .
Type 1 Lissencephaly .
X-Linked Lissencephaly .
Agyria Pachygyria Band Spectrum .
Band Heterotopia, Lissencephaly-Subcortical .
Classical Lissencephalies .
Classical Lissencephaly .
Heterotopia, Lissencephaly-Subcortical Band .
Heterotopia, Subcortical Laminar .
Heterotopias, Lissencephaly-Subcortical Band .
Heterotopias, Subcortical Band .
Heterotopias, Subcortical Laminar .
Lissencephalies, Type 1 .
Lissencephalies, X-Linked .
Lissencephaly Subcortical Band Heterotopia .
Lissencephaly Syndrome, Miller Dieker .
Lissencephaly, Classical .
Lissencephaly, Miller Dieker .
Lissencephaly, X Linked .
Lissencephaly-Subcortical Band Heterotopias .
Miller Dieker Lissencephaly Syndrome .
Miller Dieker Syndrome .
Miller-Dieker Lissencephaly .
Subcortical Band Heterotopias .
Syndrome, Double Cortex .
Syndrome, Miller-Dieker .
Syndrome, Miller-Dieker Lissencephaly .
Type 1 Lissencephalies .
X Linked Lissencephaly .
X-Linked Lissencephalies .
Heterotopia, Subcortical Band .
Lissencephalies, Classical .
Lissencephaly, Type 1 .
Lissencephaly, X-Linked .
Lissencephaly-Subcortical Band Heterotopia .
Miller-Dieker Syndrome .
Subcortical Band Heterotopia .
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.) .
0.44
3124
 
Walker-Warburg Syndrome .
COD-MD Syndrome .
Cerebroocular Dysplasia-Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Fukuyama CMD .
Fukuyama Muscular Dystrophy .
Fukuyama Syndrome .
HARD Syndrome .
Hydrocephalus, Agyria, And Retinal Dysplasia .
LGMD2K .
MDDGA1 .
MEB (Muscle-Eye-Brain) Syndrome .
Muscle Eye Brain Disease .
Muscle-Eye-Brain Disease, POMT1-Related .
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive, With Mental Retardation .
Muscular Dystrophy, Limb-Girdle, Type 2K .
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 1 .
Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 1 .
Pagon Syndrome .
CMD, Fukuyama .
COD MD Syndrome .
COD-MD Syndromes .
Cerebroocular Dysplasia Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Disease, POMT1-Related Muscle-Eye-Brain .
Diseases, POMT1-Related Muscle-Eye-Brain .
Dystrophy, Fukuyama Muscular .
HARD Syndromes .
Muscle Eye Brain Disease, POMT1 Related .
Muscle-Eye-Brain Diseases .
Muscle-Eye-Brain Diseases, POMT1-Related .
Muscular Dystrophy, Fukuyama .
POMT1-Related Muscle-Eye-Brain Disease .
POMT1-Related Muscle-Eye-Brain Diseases .
Pagon Syndromes .
Syndrome, COD-MD .
Syndrome, Chemke .
Syndrome, Fukuyama .
Syndrome, HARD .
Syndrome, Pagon .
Syndrome, Walker-Warburg .
Syndrome, Warburg .
Syndromes, COD-MD .
Syndromes, HARD .
Syndromes, Pagon .
Walker Warburg Syndrome .
alpha Dystroglycanopathies .
alpha-Dystroglycanopathies .
Cerebromuscular Dystrophy, Fukuyama Type .
Chemke Syndrome .
Fukuyama Congenital Muscular Dystrophy .
Fukuyama Type Congenital Muscular Dystrophy .
Muscle-Eye-Brain Disease .
Muscular Dystrophy, Congenital, Fukuyama Type .
Warburg Syndrome .
Rare autosomal recessive lissencephaly type 2 associated with congenital MUSCULAR DYSTROPHY and eye anomalies (e.g., RETINAL DETACHMENT; CATARACT; MICROPHTHALMOS). It is often associated with additional brain malformations such as HYDROCEPHALY and cerebellar hypoplasia and is the most severe form of the group of related syndromes (alpha-dystroglycanopathies) with common congenital abnormalities in the brain, eye and muscle development. .
0.40
293