Kagami–Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3

Omark, Jessica; Masunaga, Yohei; Hannibal, Mark C.; Shaw, Brandon; Fukami, Maki; Kato, Fumiko; Saitsu, Hirotomo; Kagami, Masayo; Ogata, Tsutomu

doi:10.1038/s10038-020-00858-x

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“…The clinical features associated with KOS due to microdeletions (Table 1) did not show a clear relation between genotype or altered gene content and described phenotype. A 15 kb common region encompassing RTL1as and MEG8 is deleted in published cases without affecting both DMRs (Omark et al, 2021). Accordingly, loss of RTL1as and the resultant RTL1 overexpression are the primary cause of KOS development.…”

Section: Discussionmentioning

confidence: 99%

Maternally inherited deletion encompassing the RTL1as and MEG8 genes of the human 14q32 imprinted region in a patient with a mild Kagami‐Ogata syndrome phenotype

Sirera

García‐Payá

Garcia

et al. 2023

American J of Med Genetics Pt A

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Kagami-Ogata syndrome and Temple syndrome are imprinting disorders caused by the abnormal expression of genes in an imprinted cluster on chromosome 14q32.Here, we report a female with mild features of the Kagami-Ogata syndrome phenotype with polyhydramnios, neonatal hypotonia, feeding difficulties, abnormal foot morphology, patent foramen ovale, distal arthrogryposis, normal facial profile, and a bell-shaped thorax without coat hanger ribs. The single nucleotide polymorphism array revealed the interstitial deletion of chromosome 14q32.2-q32.31 (117 kb in size), involving the RTL1as and MEG8 genes, and other small nucleolar RNAs and microRNAs. The differentially methylated regions (DMRs) appeared unaltered. The RTL1as gene deletion and the normal methylation pattern of the MEG3 gene loci were confirmed by methylation-specific multiplex ligation-dependent probe amplification. Deletions of the 14q32 region without involving DMRs, and encompassing only the RTL1as and MEG8 genes, are poorly described in the literature. The mother's chromosomal microarray also confirmed the identical 14q32.2 deletion, although she presented a normal phenotype. The maternally inherited 14q32 deletion was responsible for Kagami-Ogata syndrome in our patient.

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Section: Discussionmentioning

confidence: 99%