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Molecular Medicine Reports
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Print ISSN: 1791-2997 Online ISSN: 1791-3004
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August-2018 Volume 18 Issue 2

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Case Report

Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report

  • Authors:
    • Wenjin Yan
    • Jin Dai
    • Dongquan Shi
    • Xingquan Xu
    • Xiao Han
    • Zhihong Xu
    • Dongyang Chen
    • Huajiang Teng
    • Qing Jiang
  • View Affiliations / Copyright

    Affiliations: Department of Sports Medicine and Adult Reconstructive Surgery, Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, Jiangsu 210008, P.R. China, Laboratory for Bone and Joint Disease, Model Animal Research Center (MARC), Nanjing University, Nanjing, Jiangsu 210093, P.R. China
  • Pages: 1761-1765
    |
    Published online on: June 6, 2018
       https://doi.org/10.3892/mmr.2018.9143
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Abstract

Schwartz-Jampel syndrome type 1 (SJS1) is a rare autosomal recessive disease caused by mutations in the gene heparan sulfate proteoglycan 2 (HSPG2; also known as basement membrane‑specific heparin sulfate). In the present study, a 10‑year‑old female SJS1 proband from a Chinese family, who was diagnosed by X‑ray and physical examination, was recruited. The key clinical features of the patient with SJS1 included short stature, joint contractures, pigeon breast, and myotonia that led to progressive stiffness of the face and limbs; barely discernible kyphosis was also noted. Genetic testing using whole exome sequencing and Sanger sequencing was performed for the proband and family members. A total of 2 novel mutations (c.8788G>A; p.Glu2930Lys and c.11671+5G>A) in the HSPG2 gene were identified in the proband. The family members harboring 1 heterozygous mutation in HSPG2 did not exhibit any skeletal abnormalities. The results of the present study suggested that the compound heterozygous mutations in HSPG2 may be responsible the induction of SJS1, and demonstrated the genotype‑phenotype associations between mutations in the HSPG2 gene and clinical characteristics of SJS1.
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Copy and paste a formatted citation
Spandidos Publications style
Yan W, Dai J, Shi D, Xu X, Han X, Xu Z, Chen D, Teng H and Jiang Q: Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report. Mol Med Rep 18: 1761-1765, 2018.
APA
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z. ... Jiang, Q. (2018). Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report. Molecular Medicine Reports, 18, 1761-1765. https://doi.org/10.3892/mmr.2018.9143
MLA
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z., Chen, D., Teng, H., Jiang, Q."Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report". Molecular Medicine Reports 18.2 (2018): 1761-1765.
Chicago
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z., Chen, D., Teng, H., Jiang, Q."Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report". Molecular Medicine Reports 18, no. 2 (2018): 1761-1765. https://doi.org/10.3892/mmr.2018.9143
Copy and paste a formatted citation
x
Spandidos Publications style
Yan W, Dai J, Shi D, Xu X, Han X, Xu Z, Chen D, Teng H and Jiang Q: Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report. Mol Med Rep 18: 1761-1765, 2018.
APA
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z. ... Jiang, Q. (2018). Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report. Molecular Medicine Reports, 18, 1761-1765. https://doi.org/10.3892/mmr.2018.9143
MLA
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z., Chen, D., Teng, H., Jiang, Q."Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report". Molecular Medicine Reports 18.2 (2018): 1761-1765.
Chicago
Yan, W., Dai, J., Shi, D., Xu, X., Han, X., Xu, Z., Chen, D., Teng, H., Jiang, Q."Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report". Molecular Medicine Reports 18, no. 2 (2018): 1761-1765. https://doi.org/10.3892/mmr.2018.9143
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