A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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Single-Gene Determinants of Epilepsy Comorbidity.FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.Lennox-Gastaut syndrome: a comprehensive review.

P2860

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P2860

A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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P1476

A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

@en

P2093

Bertrand Diebold

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Catherine Delanoe

http://www.w3.org/2001/XMLSchema#string

David Germanaud

http://www.w3.org/2001/XMLSchema#string

Gaetano Terrone

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Marie-Anne Barthez-Carpentier

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Thierry Bienvenu

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P2860

De novo mutations in epileptic encephalopathies

FOXG1 is responsible for the congenital variant of Rett syndrome

Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres

Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon.

A FOXG1 mutation in a boy with congenital variant of Rett syndrome.

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.

Lennox-Gastaut syndrome (childhood epileptic encephalopathy).

Copy number variants in adult patients with Lennox-Gastaut syndrome features.

Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.

Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology.

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e116-9

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scholarly article

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10.1111/EPI.12800

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P433

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P478

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Sandrine Passemard

Stéphane Auvin

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2014-09-29T00:00:00Z

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P698

25266269

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A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

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P2860

P2860

A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698