Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicism
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- 作者：Shahida Moosa ; Helena Bö ; hrer-Rabel ; Janine Altmü ; ller ; Filippo Beleggia ; Peter Nü ; rnberg ; Yun Li ; Gö ; khan Yigit and Bernd Wollnik
- 刊名：American Journal of Medical Genetics Part A
- 出版年：2017
- 出版时间：January 2017
- 年：2017
- 卷：173
- 期：1
- 页码：264-267
- 全文大小：360K
- ISSN：1552-4833
文摘
Heterozygous germline mutations in MTOR have been shown to underlie Smith–Kingsmore syndrome, a rare autosomal dominant syndrome characterized by macrocephaly, developmental delay, and dysmorphic facial features. Recently, two unrelated families with the MTOR mutation, c.5395G>A p.(Glu1799Lys), were reported. Here, we describe siblings from a non-consanguineous German family in whom we identified the same heterozygous missense mutation in MTOR. Remarkably, in all reported families with Smith–Kingsmore syndrome and the MTOR c.5395G>A mutation, including the family described herein, healthy parents of recurrently affected children do not have detectable levels of the mutation in tested tissues, lending credence to gonadal mosaicism as the underlying mechanism. Furthermore, the glutamic acid at position 1799 was shown to present a recurrent somatic mutation site in several cancers, including colon cancer, pointing to a somatic mutational hotspot in MTOR. Importantly, we highlight the occurrence of multiple intestinal polyps in the older sibling. Further patients are required to establish definitively whether polyp formation forms part of the SKS clinical spectrum.