TY - JOUR
T1 - Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing
AU - Berger, Itai
AU - Ben-Neriah, Ziva
AU - Dor-Wolman, Talia
AU - Shaag, Avraham
AU - Saada, Ann
AU - Zenvirt, Shamir
AU - Raas-Rothschild, Annick
AU - Nadjari, Michel
AU - Kaestner, Klaus H.
AU - Elpeleg, Orly
N1 - Funding Information:
We are grateful to Chaim Jalas at Bonei Olam Center for Rare Jewish Genetic Disorders, Brooklyn, NY for bioinformatic analysis, and to Alan J. Fox and Dr. Jonathan Schug for exome sequencing. The excellent technical assistance of Lital Sheva is greatly appreciated. This work was funded in part by Association Myologie Francaise (AFM) and by the Israeli Ministry of Health grant # 5914 .
PY - 2011/12
Y1 - 2011/12
N2 - The identification of disease causing mutation in patients with neurodegenerative disorders originating from small, non-consanguineous families is challenging. Three siblings were found to have ventriculomegaly at early gestation; postnatally, there was no acquisition of developmental milestones, and the muscles of the children were dystrophic. Plasma and CSF lactate levels were normal, but the activities of mitochondrial complex I and IV were markedly decreased. Using linkage analysis in the family, followed by whole exome sequencing of a single patient, we identified a pathogenic mutation in the AIFM1 gene which segregated with the disease state and was absent in 86 anonymous controls. This is the second report of a mutation in the AIFM1 gene, extending the clinical spectrum to include prenatal ventriculomegaly and underscores the importance of AIF for complex I assembly. In summary, linkage analysis followed by exome sequencing of a single patient is a cost-effective approach for the identification of disease causing mutations in small non-consanguineous families.
AB - The identification of disease causing mutation in patients with neurodegenerative disorders originating from small, non-consanguineous families is challenging. Three siblings were found to have ventriculomegaly at early gestation; postnatally, there was no acquisition of developmental milestones, and the muscles of the children were dystrophic. Plasma and CSF lactate levels were normal, but the activities of mitochondrial complex I and IV were markedly decreased. Using linkage analysis in the family, followed by whole exome sequencing of a single patient, we identified a pathogenic mutation in the AIFM1 gene which segregated with the disease state and was absent in 86 anonymous controls. This is the second report of a mutation in the AIFM1 gene, extending the clinical spectrum to include prenatal ventriculomegaly and underscores the importance of AIF for complex I assembly. In summary, linkage analysis followed by exome sequencing of a single patient is a cost-effective approach for the identification of disease causing mutations in small non-consanguineous families.
KW - Anti-apoptotic factor
KW - Complex I deficiency
KW - Ventriculomegaly
UR - http://www.scopus.com/inward/record.url?scp=82255162594&partnerID=8YFLogxK
U2 - 10.1016/j.ymgme.2011.09.020
DO - 10.1016/j.ymgme.2011.09.020
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C2 - 22019070
AN - SCOPUS:82255162594
SN - 1096-7192
VL - 104
SP - 517
EP - 520
JO - Molecular Genetics and Metabolism
JF - Molecular Genetics and Metabolism
IS - 4
ER -