| Descriptor English: | Classical Lissencephalies and Subcortical Band Heterotopias | ||||||
| Descriptor Spanish: |
Lisencefalias Clásicas y Heterotopias Subcorticales en Banda
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| Descriptor Portuguese: | Lissencefalias Clássicas e Heterotopias Subcorticais em Banda | ||||||
| Descriptor French: | Lissencéphalies classiques et hétérotopies laminaires sous-corticales | ||||||
| Entry term(s): |
1, Lissencephaly 1, Lissencephaly Type 1s, Lissencephaly 1s, Lissencephaly Type Agyria Pachygyria Band Spectrum Agyria-Pachygyria-Band Spectrum Band Heterotopia, Lissencephaly-Subcortical Chromosome 17p13.3 Deletion Syndrome Classic Lissencephalies Classic Lissencephaly Classical Lissencephalies Classical Lissencephaly Classical Lissencephaly Syndrome Classical Lissencephaly Syndromes Double Cortex Syndrome Heterotopia, Lissencephaly-Subcortical Band Heterotopia, Subcortical Band Heterotopia, Subcortical Laminar Heterotopias, Lissencephaly-Subcortical Band Heterotopias, Subcortical Band Heterotopias, Subcortical Laminar Isolated Lissencephaly Sequence Lissencephalies, Classic Lissencephalies, Classical Lissencephalies, Type 1 Lissencephalies, X-Linked Lissencephaly 1 Lissencephaly 1s Lissencephaly Sequence, Isolated Lissencephaly Subcortical Band Heterotopia Lissencephaly Syndrome, Classical Lissencephaly Syndrome, Miller Dieker Lissencephaly Syndrome, Miller-Dieker Lissencephaly Syndromes, Classical Lissencephaly Type 1 Lissencephaly Type 1s Lissencephaly, Classic Lissencephaly, Classical Lissencephaly, Miller Dieker Lissencephaly, Miller-Dieker Lissencephaly, Type 1 Lissencephaly, X Linked Lissencephaly, X-Linked Lissencephaly, X-Linked, 1 Lissencephaly-Subcortical Band Heterotopia Lissencephaly-Subcortical Band Heterotopias Miller Dieker Lissencephaly Syndrome Miller Dieker Syndrome Miller-Dieker Lissencephaly Miller-Dieker Lissencephaly Syndrome Miller-Dieker Syndrome Subcortical Band Heterotopia Subcortical Band Heterotopias Subcortical Laminar Heterotopia Syndrome, Classical Lissencephaly Syndrome, Double Cortex Syndrome, Miller-Dieker Syndrome, Miller-Dieker Lissencephaly Syndromes, Classical Lissencephaly Type 1 Lissencephalies Type 1 Lissencephaly Type 1, Lissencephaly Type 1s, Lissencephaly X Linked Lissencephaly X-Linked Lissencephalies X-Linked Lissencephaly |
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| Tree number(s): |
C10.500.507.450.230 C10.500.507.450.499.230 C16.131.666.507.450.230 C16.131.666.507.450.499.230 C16.320.322.500.186 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D054221 | ||||||
| Scope note: | 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.) |
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| 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 |
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| Previous Indexing: |
Cerebral Cortex/abnormalities (1993-2007) |
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| Public MeSH Note: | 2008 |
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| History Note: | 2008 |
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| DeCS ID: | 52595 | ||||||
| Unique ID: | D054221 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2008/01/01 | ||||||
| Date of Entry: | 2007/07/09 | ||||||
| Revision Date: | 2018/10/10 |
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Classical Lissencephalies and Subcortical Band Heterotopias
- Preferred
Lissencephaly Syndrome, Miller-Dieker
- Narrower
X-Linked Lissencephaly
- Narrower
Lissencephalies, Classical
- Narrower
Subcortical Band Heterotopia
- Narrower
Lissencephaly, X-Linked, 1
- Narrower
| Concept UI |
M0501375 |
| Scope note | 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.) |
| Preferred term | Classical Lissencephalies and Subcortical Band Heterotopias |
| Entry term(s) |
Agyria Pachygyria Band Spectrum Agyria-Pachygyria-Band Spectrum Band Heterotopia, Lissencephaly-Subcortical Heterotopia, Lissencephaly-Subcortical Band Heterotopias, Lissencephaly-Subcortical Band Lissencephaly Subcortical Band Heterotopia Lissencephaly-Subcortical Band Heterotopia Lissencephaly-Subcortical Band Heterotopias |
| Concept UI |
M0501377 |
| Preferred term | Lissencephaly Syndrome, Miller-Dieker |
| Entry term(s) |
Chromosome 17p13.3 Deletion Syndrome Lissencephaly Syndrome, Miller Dieker Lissencephaly, Miller Dieker Lissencephaly, Miller-Dieker Miller Dieker Lissencephaly Syndrome Miller Dieker Syndrome Miller-Dieker Lissencephaly Miller-Dieker Lissencephaly Syndrome Miller-Dieker Syndrome Syndrome, Miller-Dieker Syndrome, Miller-Dieker Lissencephaly |
| Concept UI |
M0501379 |
| Preferred term | X-Linked Lissencephaly |
| Entry term(s) |
Lissencephalies, X-Linked Lissencephaly, X Linked Lissencephaly, X-Linked X Linked Lissencephaly X-Linked Lissencephalies |
| Concept UI |
M0503208 |
| Preferred term | Lissencephalies, Classical |
| Entry term(s) |
1, Lissencephaly 1, Lissencephaly Type 1s, Lissencephaly 1s, Lissencephaly Type Classic Lissencephalies Classic Lissencephaly Classical Lissencephalies Classical Lissencephaly Classical Lissencephaly Syndrome Classical Lissencephaly Syndromes Isolated Lissencephaly Sequence Lissencephalies, Classic Lissencephalies, Type 1 Lissencephaly 1 Lissencephaly 1s Lissencephaly Sequence, Isolated Lissencephaly Syndrome, Classical Lissencephaly Syndromes, Classical Lissencephaly Type 1 Lissencephaly Type 1s Lissencephaly, Classic Lissencephaly, Classical Lissencephaly, Type 1 Syndrome, Classical Lissencephaly Syndromes, Classical Lissencephaly Type 1 Lissencephalies Type 1 Lissencephaly Type 1, Lissencephaly Type 1s, Lissencephaly |
| Concept UI |
M0501378 |
| Preferred term | Subcortical Band Heterotopia |
| Entry term(s) |
Double Cortex Syndrome Heterotopia, Subcortical Band Heterotopia, Subcortical Laminar Heterotopias, Subcortical Band Heterotopias, Subcortical Laminar Subcortical Band Heterotopias Subcortical Laminar Heterotopia Syndrome, Double Cortex |
| Concept UI |
M000644374 |
| Preferred term | Lissencephaly, X-Linked, 1 |
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