These authors contributed equally to this work.
Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations
Article first published online: 26 JUL 2013
© 2013 WILEY PERIODICALS, INC.
Volume 34, Issue 10, pages 1381–1386, October 2013
How to Cite
Iida, A., Simsek-Kiper, P. Ö., Mizumoto, S., Hoshino, T., Elcioglu, N., Horemuzova, E., Geiberger, S., Yesil, G., Kayserili, H., Utine, G. E., Boduroglu, K., Watanabe, S., Ohashi, H., Alanay, Y., Sugahara, K., Nishimura, G. and Ikegawa, S. (2013), Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations. Hum. Mutat., 34: 1381–1386. doi: 10.1002/humu.22377
Communicated by Ming Qi
Contract grant sponsors: Ministry of Health, Labor and Welfare (23300101 to S.I. and N.M., 23300201 to S.I.); Matching Program for Innovations in Future Drug Discovery and Medical Care, The Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT) (to K.S.); Grant-in-aid for Young Scientists (B) (23790066), The Japan Society for the Promotion of Science, Japan (to S.M.); The Japan Heart Foundation (to S.M.); Akiyama Life Science Foundation (to S.M.).
- Issue published online: 18 SEP 2013
- Article first published online: 26 JUL 2013
- Accepted manuscript online: 3 JUL 2013 02:17PM EST
- Manuscript Accepted: 25 JUN 2013
- Manuscript Received: 6 APR 2013
- Ministry of Health, Labor and Welfare. Grant Numbers: 23300101, 23300201
- Matching Program for Innovations in Future Drug Discovery and Medical Care
- The Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT)
- Grant-in-aid for Young Scientists. Grant Number: 23790066
- The Japan Society for the Promotion of Science, Japan
- The Japan Heart Foundation
- Akiyama Life Science Foundation
- androgen excess
Brachyolmia is a heterogeneous skeletal dysplasia characterized by generalized platyspondyly without significant long-bone abnormalities. Based on the mode of inheritance and radiographic features, at least three types of brachyolmia have been postulated. We recently identified an autosomal recessive form of brachyolmia that is caused by loss-of-function mutations of PAPSS2, the gene encoding PAPS (3′-phosphoadenosine 5′-phosphosulfate) synthase 2. To understand brachyolmia caused by PAPSS2 mutations (PAPSS2-brachyolmia), we extended our PAPSS2 mutation analysis to 13 patients from 10 families and identified homozygous or compound heterozygous mutations in all. Nine different mutations were found: three splice donor-site mutations, three missense mutations, and three insertion or deletion mutations within coding regions. In vitro enzyme assays showed that the missense mutations were also loss-of-function mutations. Phenotypic characteristics of PAPSS2-brachyolmia include short-trunk short stature, normal intelligence and facies, spinal deformity, and broad proximal interphalangeal joints. Radiographic features include platyspondyly with rectangular vertebral bodies and irregular end plates, broad ilia, metaphyseal changes of the proximal femur, including short femoral neck and striation, and dysplasia of the short tubular bones. PAPSS2-brachyolmia includes phenotypes of the conventional clinical concept of brachyolmia, the Hobaek and Toledo types, and is associated with abnormal androgen metabolism.