Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27.

American journal of medical genetics. Part A - 1 May 2008

Santos Neide F, Secolin Rodrigo, Brandão-Almeida Iara L, Silva Marilza S, Torres Fábio R, Tsuneda Simone S, Guimarães Catarina A, Hage Simone R V, Cendes Fernando, Guerreiro Marilisa M, Lopes-Cendes Iscia

Abstract excerpt

Polymicrogyria (PMG) is characterized by an excessive number of small and prominent brain gyri, separated by shallow sulci. Bilateral perisylvian polymicrogyria (BPP) is the most common form of PMG. Clinical signs include pseudobulbar paresis, mental retardation, and epilepsy. Familial forms of B...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cerebral Cortex
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, X

Share to Haplotypes

Share to Lod Score

Share to Magnetic Resonance Imaging

Share to Malformations of Cortical Development

Share to Microsatellite Repeats

Source

Identifiers

PMID: 18384144
DOI: 10.1002/ajmg.a.32270

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18384144-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27.PMID 18384144Read ↗

Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.Semantic proximity Read ↗

Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16Semantic proximity Read ↗

Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopmentSemantic proximity Read ↗

Duplication 2p16 is associated with perisylvian polymicrogyria.Semantic proximity Read ↗

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.Semantic proximity Read ↗

Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation.Semantic proximity Read ↗

X-Linked Bilateral Polymicrogyria With Epilepsy and Intellectual Disability Associated With a Novel KIF4A Variant.Semantic proximity Read ↗

Familial and genetic associations in Worster-Drought syndrome and perisylvian disorders.Semantic proximity Read ↗

A gene for ataxic cerebral palsy maps to chromosome 9p12-q12.Semantic proximity Read ↗

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.Semantic proximity Read ↗

A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.Semantic proximity Read ↗

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical DevelopmentSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.