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Genomic screening in rare disorders: new mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability
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2018 (Engelska)Ingår i: Clinical Genetics, ISSN 0009-9163, E-ISSN 1399-0004, Vol. 94, nr 6, s. 528-537Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We have investigated 20 consanguineous families with multiple children affected by rare disorders. Detailed clinical examinations, exome sequencing of affected as well as unaffected family members and further validation of likely pathogenic variants were performed. In 16/20 families, we identified pathogenic variants in autosomal recessive disease genes (ALMS1, PIGT, FLVCR2, TFG, CYP7B1, ALG14, EXOSC3, MEGF10, ASAH1, WDR62, ASPM, PNPO, ERCC5, KIAA1109, RIPK4, MAN1B1). A number of these genes have only rarely been reported previously and our findings thus confirm them as disease genes, further delineate the associated phenotypes and expand the mutation spectrum with reports of novel variants. We highlight the findings in two affected siblings with splice altering variants in ALG14 and propose a new clinical entity, which includes severe intellectual disability, epilepsy, behavioral problems and mild dysmorphic features, caused by biallelic variants in ALG14.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2018. Vol. 94, nr 6, s. 528-537
Nyckelord [en]
ALG14, exome sequencing, genome screening, intellectual disability, KIAA1109, rare disorders
Nationell ämneskategori
Medicinsk genetik
Identifikatorer
URN: urn:nbn:se:umu:diva-154933DOI: 10.1111/cge.13448ISI: 000450028600005PubMedID: 30221345OAI: oai:DiVA.org:umu-154933DiVA, id: diva2:1275714
Forskningsfinansiär
Knut och Alice Wallenbergs StiftelseStockholms läns landstingTillgänglig från: 2019-01-07 Skapad: 2019-01-07 Senast uppdaterad: 2019-01-07Bibliografiskt granskad

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Burstedt, Magnus

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Taylan, FulyaNilsson, DanielBurstedt, Magnus
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Medicinsk och klinisk genetik
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Clinical Genetics
Medicinsk genetik

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