Lissencephaly Latest Advances

Find the Latest Research About Lissencephaly

Last Updated: 09/26/2026

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Found 974 publications

Genotype-Driven MRI Re-evaluation Reveals Subtle PAFAH1B1-Related Lissencephaly.

Genotype-Driven MRI Re-evaluation Reveals Subtle PAFAH1B1-Related Lissencephaly.

Journal: Journal of child neurology
Published: August 27, 2026

Biallelic Frameshift Variant in LAMB1 Associated with Occipital Meningoencephalocele and Pansutural Craniosynostosis: A Case Report and Review of the Literature.

Biallelic Frameshift Variant in LAMB1 Associated with Occipital Meningoencephalocele and Pansutural Craniosynostosis: A Case Report and Review of the Literature.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
Published: August 13, 2026

Expanding the Neuroimaging Spectrum of 17p13.3 Deletions: Lissencephaly with Cerebellar Hypoplasia as a Novel Phenotype.

Expanding the Neuroimaging Spectrum of 17p13.3 Deletions: Lissencephaly with Cerebellar Hypoplasia as a Novel Phenotype.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: July 28, 2026

Clinical Spectrum and Genetics of Ocular Manifestations in Muscle Eye Brain Disease: A Literature Review.

Clinical Spectrum and Genetics of Ocular Manifestations in Muscle Eye Brain Disease: A Literature Review.

Journal: Seminars in ophthalmology
Published: June 29, 2026

Genetic causes of the lissencephaly spectrum: insights from chromosomal microarray and clinical/whole-exome sequencing.

Genetic causes of the lissencephaly spectrum: insights from chromosomal microarray and clinical/whole-exome sequencing.

Journal: Croatian medical journal
Published: June 13, 2026

Corpus Callosotomy in LIS1 Lissencephaly: Postoperative Ketogenic Diet-Related Metabolic Derangements and Feeding Intolerance.

Corpus Callosotomy in LIS1 Lissencephaly: Postoperative Ketogenic Diet-Related Metabolic Derangements and Feeding Intolerance.

Journal: Cureus
Published: June 12, 2026

DCX-associated lissencephaly

DCX-associated lissencephaly

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: May 14, 2026

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Journal: Prenatal diagnosis
Published: May 07, 2026

Novel Homozygous TUBGCP6 Variant Impairs Brain Development: Case Report and Literature Review.

Novel Homozygous TUBGCP6 Variant Impairs Brain Development: Case Report and Literature Review.

Journal: Journal of child neurology
Published: April 25, 2026

Miller-Dieker Syndrome: Genetic Etiology, Neurocognitive Impact, and Clinical Implications in a Neuronal Migration Disorder.

Miller-Dieker Syndrome: Genetic Etiology, Neurocognitive Impact, and Clinical Implications in a Neuronal Migration Disorder.

Journal: Developmental neuropsychology
Published: April 14, 2026

Non-transport functions of motor proteins in corticogenesis.

Non-transport functions of motor proteins in corticogenesis.

Journal: Frontiers in cell and developmental biology
Published: March 30, 2026

Expanding the Genotypic Spectrum of POMGNT1-Related Muscle-Eye-Brain Disease: A Case Report.

Expanding the Genotypic Spectrum of POMGNT1-Related Muscle-Eye-Brain Disease: A Case Report.

Journal: Molecular genetics & genomic medicine
Published: March 20, 2026
Showing 1-12 of 974

Last Updated: 09/26/2026