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

Lissencephaly with Congenital Hypothyroidism: A Case Report.

JNMA; journal of the Nepal Medical Association - 2 Nov 2022

Sahani Shambhu Kumar, Pathak Anil, Nepali Bishal, Rai Nilshan

Abstract excerpt

Lissencephaly is a malformation of cortical development associated with deficient neuronal migration and abnormal formation of cerebral convolutions or gyri. The lissencephaly spectrum consists of agyria, pachygyria, and subcortical band heterotopia. At least 19 genes have been identified in the causation of lissencephaly and related syndrome. Lissencephaly is associated with many other congenital disorders but...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Congenital Hypothyroidism
Share to Lissencephaly

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 36705174
DOI: 10.31729/jnma.7893
PMCID: PMC9795095

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lissencephaly with Congenital Hypothyroidism: A Case Report.PMID 36705174Read ↗

Lissencephaly: Update on diagnostics and clinical management.Semantic proximity Read ↗

The genetics of lissencephaly.Semantic proximity Read ↗

The clinical patterns and molecular genetics of lissencephaly and subcortical band heterotopiaSemantic proximity Read ↗

Lissencephaly: Expanded imaging and clinical classification.Semantic proximity Read ↗

Lissencephaly and Other Malformations of Cortical Development: 1995 UpdateSemantic proximity Read ↗

Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.Semantic proximity Read ↗

Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.Semantic proximity Read ↗

Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.Semantic proximity Read ↗

A 14-year-old girl with lissencephaly and craniofacial dysmorphism.Semantic proximity Read ↗

Genetic Basis of Brain MalformationsSemantic proximity Read ↗

Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasiasSemantic proximity Read ↗

Malformations of cortical development.Semantic proximity Read ↗

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