Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities.

TitleMutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities.
Publication TypeJournal Article
Year of Publication2013
AuthorsRadmanesh, F, Çağlayan, AOkay, Silhavy, JL, Yilmaz, C, Cantagrel, V, Omar, T, Rosti, B, Kaymakçalan, H, Gabriel, S, Li, M, Šestan, N, Bilguvar, K, Dobyns, WB, Zaki, MS, Günel, M, Gleeson, JG
JournalAm J Hum Genet
Volume92
Issue3
Pagination468-74
Date Published2013 Mar 07
ISSN1537-6605
KeywordsBasement Membrane, Brain, Cerebellum, Cerebral Cortex, Encephalocele, Female, Genetic Predisposition to Disease, Homozygote, Humans, Laminin, Male, Muscular Dystrophies, Nervous System Malformations, Neuroglia, Neurons, Sequence Deletion, Walker-Warburg Syndrome
Abstract

Cobblestone brain malformation (COB) is a neuronal migration disorder characterized by protrusions of neurons beyond the first cortical layer at the pial surface of the brain. It is usually seen in association with dystroglycanopathy types of congenital muscular dystrophies (CMDs) and ocular abnormalities termed muscle-eye-brain disease. Here we report homozygous deleterious mutations in LAMB1, encoding laminin subunit beta-1, in two families with autosomal-recessive COB. Affected individuals displayed a constellation of brain malformations including cortical gyral and white-matter signal abnormalities, severe cerebellar dysplasia, brainstem hypoplasia, and occipital encephalocele, but they had less apparent ocular or muscular abnormalities than are typically observed in COB. LAMB1 is localized to the pial basement membrane, suggesting that defective connection between radial glial cells and the pial surface mediated by LAMB1 leads to this malformation.

DOI10.1016/j.ajhg.2013.02.005
Alternate JournalAm. J. Hum. Genet.
PubMed ID23472759
PubMed Central IDPMC3591846
Grant ListU01MH081896 / MH / NIMH NIH HHS / United States
U54 HG003067 / HG / NHGRI NIH HHS / United States
P30NS047101 / NS / NINDS NIH HHS / United States
R01NS048453 / NS / NINDS NIH HHS / United States
P30 NS047101 / NS / NINDS NIH HHS / United States
U54HG003067 / HG / NHGRI NIH HHS / United States
RC2 NS070477 / NS / NINDS NIH HHS / United States
R01 NS048453 / NS / NINDS NIH HHS / United States
U54HG006504 / HG / NHGRI NIH HHS / United States
U54 HG006504 / HG / NHGRI NIH HHS / United States
RC2NS070477 / NS / NINDS NIH HHS / United States
U01 MH081896 / MH / NIMH NIH HHS / United States
R01 NS052455 / NS / NINDS NIH HHS / United States
P01 HD070494 / HD / NICHD NIH HHS / United States
/ / Howard Hughes Medical Institute / United States
P01HD070494 / HD / NICHD NIH HHS / United States
R01NS052455 / NS / NINDS NIH HHS / United States