Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome.
10.3881/j.issn.1000-503X.12629
- Author:
Zi Quan LI
1
;
Mo Zhao GENG
1
;
Sen ZHAO
1
;
Zhi Hong WU
2
;
Jian Guo ZHANG
1
;
Nan WU
1
;
Yi Peng WANG
1
Author Information
1. Department of Orthopaedics, PUMC Hospital, CANS and PUMC, Beiig 10730 China.
2. Beijing Key Laboratory for Genetic Research of Skeletal Deformity,PUMC Hospital, CANS and PUMC, Beiig 10730 China.
- Publication Type:Journal Article
- Keywords:
Klippel-Feil syndrome;
associated anomalies;
clinical triad;
gene mutation;
multigene panel sequencing
- MeSH:
Cervical Vertebrae;
Child;
Cohort Studies;
Female;
Glycoproteins;
Humans;
Klippel-Feil Syndrome/genetics*;
Male;
Mutation;
Nuclear Proteins;
Radiography;
Transcription Factors/genetics*
- From:
Acta Academiae Medicinae Sinicae
2021;43(1):25-31
- CountryChina
- Language:Chinese
-
Abstract:
Objective To summarize clinical characteristics and investigate possible pathogenic gene of Klippel-Feil syndrome(KFS)by the self-designed multigene panel sequencing,so as to decipher the molecular basis for early diagnosis and targeted therapy.Methods From January 2015 to December 2018,we consecutively recruited 25 patients who were diagnosed with KFS in Peking Union Medical College Hospital.The demographic information,clinical manifestations,physical examination and radiological assessments were analyzed.Multigene panel sequencing was performed after DNA extraction from peripheral blood.The possible pathogenic mutations of KFS were explored on the basis of bioinformatics analysis.Results The KFS cohort consisted of 25 patients,including 15 males and 10 females,with a mean age of(12.9±7.3)years.Limited cervical range of motion was the most common clinical feature(12 cases,48%).Based on the Samartzis classification,the proportion of patients suffered from short neck(P=0.031)and limited cervical range of motion(P=0.026)in type Ⅲ KFS was significantly higher than that in type Ⅱ and type Ⅰ KFS.Panel sequencing detected a total of 11 pathogenic missense mutations in eight patients,including COL6A1,COL6A2,CDAN1,GLI3,FLNB,CHRNG,MYH3,POR,and TNXB.There was no pathogenic mutation found in five reported pathogenic genes(GDF6,MEOX1,GDF3,MYO18B and RIPPLY2)associated with KFS.Conclusions Our study has shown that patients with multiple contiguous cervical fusions are more likely to manifest short neck,limited cervical range of motion,and clinical triad.Therefore,these patients need additional attention and follow-up.Our analysis highlights novel KFS-related genetic variants,such as COL6A and CDAN1,extending the spectrum of known mutations contributing to this syndrome and providing a basis for elucidating the pathogenesis of KFS.
