A new case of Smith‐Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth
A new case of Smith‐Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth
复制标题
带有体细胞 MTOR 致病性变异的 Smith-Kingsmore 综合征新病例将表型谱扩展到偏侧过度生长
DOI:
10.1111/cge.13931
复制
发表时间:
2021
影响因子:
3.5
通讯作者:
A. Mussa
中科院分区:
文献类型:
--
作者:
D. Carli;G. Ferrero;Anna Fusillo;P. Coppo;Roberta La Selva;F. Zinali;S. Cardaropoli;C. Ranieri;M. Iacoviello;N. Resta;A. Mussa
Smith‐Kingsmore syndrome (SKS) is a rare autosomal dominant disorder caused by heterozygous germline activating pathogenic variants in mammalian target of rapamycin (MTOR) on chromosome 1p36. A few patients with disseminated mosaicism have been described so far and they seem to display a different phenotype when compared to germline cases. Here we report the sixth case with a disseminated mosaic MTOR pathogenic variant, a 7‐year‐old boy with hemimegalencephaly, epilepsy, developmental delay, hypomelanosis of Ito, and lateralized overgrowth. Genetic testing revealed a pathogenic variant (c.4448G > A, p.Cys1483Tyr) in MTOR with a frequency of 32% in the DNA extracted from a skin sample, 3% in saliva and 0.46% in blood. The clinical features observed in our patient further corroborate the existence of differences in phenotypic presentation of germline and mosaic SKS cases. Moreover, lateralized overgrowth, a finding never described so far in SKS, further expands the phenotypic spectrum of SKS and allows the inclusion of MTOR pathogenic variants among the several causes of asymmetric body overgrowth.
影响因子:
29
作者:
Mirzaa GM;Campbell CD;Solovieff N;Goold C;Jansen LA;Menon S;Timms AE;Conti V;Biag JD;Adams C;Boyle EA;Collins S;Ishak G;Poliachik S;Girisha KM;Yeung KS;Chung BHY;Rahikkala E;Gunter SA;McDaniel SS;Macmurdo CF;Bernstein JA;Martin B;Leary R;Mahan S;Liu S;Weaver M;Doerschner M;Jhangiani S;Muzny DM;Boerwinkle E;Gibbs RA;Lupski JR;Shendure J;Saneto RP;Novotny EJ;Wilson CJ;Sellers WR;Morrissey M;Hevner RF;Ojemann JG;Guerrini R;Murphy LO;Winckler W;Dobyns WB
通讯作者:
Dobyns WB