Smith-Kingsmore syndrome caused by MTOR gene variation: 2 cases and literature review.
10.3760/cma.j.cn112140-20220321-00226
- VernacularTitle:MTOR基因变异致Smith-Kingsmore综合征2例并文献复习
- Author:
Hai Hong LEI
1
;
Li Li LIU
1
;
Qiong WANG
1
;
Xiao Ling TIE
1
;
Xiao Cui TIAN
1
;
Nan JI
1
;
Ying YANG
2
Author Information
1. Department of Rehabilitation, Xi'an Children's Hospital, Xi'an 710002, China.
2. Shaanxi Institute for Pediatric Diseases, Xi'an Children's Hospital, Xi'an 710002, China.
- Publication Type:Review
- MeSH:
Autism Spectrum Disorder;
Female;
Humans;
Hypoglycemia;
Intellectual Disability/genetics*;
Megalencephaly/genetics*;
Muscle Hypotonia;
Mutation;
Retrospective Studies;
TOR Serine-Threonine Kinases/genetics*
- From:
Chinese Journal of Pediatrics
2022;60(9):935-939
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the clinical manifestations and genetic features of 2 children with Smith-Kingsmore syndrome caused by MTOR gene variation and review the literature. Methods: The clinical data of 2 children carrying MTOR gene variant, diagnosed at Xi'an Children's Hospital from April 2018 to April 2021, were retrospectively summarized."MTOR"and"Smith-Kingsmore syndrome"were used as key words to search at China National Knowledge Infrastructure, Wanfang Data Knowledge Service Platform, PubMed and OMIM up to August 2021. The characteristics of MTOR gene variation and the clinical phenotype of children with Smith-Kingsmore syndrome were summarized. Results: Two children were both females, aged 1.5 years and 2 years respectively, the onset age were both in infancy. They both had developmental delay, megalencephaly and abnormal face. Both whole exome sequencing revealed a de novo heterozygous missense variant in MTOR gene. One case carried c.5395G>A (p.Glu1799Lys) and the other case carried c.7234G>C (p.Asp2412His). There was no literature of MTOR gene variation in Chinese. So far, a total of 45 cases were reported worldwide with detailed clinical information. Eleven variations in MTOR gene were involved, which were all heterozygous missense mutations. Among them, p.Glu1799Lys was the most common sites (28 cases,62%). Another case carried c.7234G>C (p.Asp2412His) was not reported before. Summarizing the 47 cases (including these 2 cases), 46 cases had developmental delay or intellectual disability, 9 cases had developmental regression,42 cases had megalencephaly, 30 cases had facial malformation,16 cases had hypotonia, 17 cases had autism spectrum disorders, 3 cases had hyperactivity, 3 cases had obsessive compulsive disorder, 13 cases had eye diseases, 11 cases had cutaneous vascular malformation, and 9 cases had hypoglycemia. Conclusions: The main clinical features of Smith-Kingsmore syndrome include megalencephaly, developmental delay or intellectual disability, and facial malformation, which can be combined with epilepsy, autism spectrum disorder, hypotonia, hypoglycemia and so on. The variation of MTOR gene is the cause of Smith-Kingsmore syndrome.
