Analysis of clinical manifestations and treatment in 26 children with fibrodysplasia ossificans progressiva in China-Reference-Cited by-同舟云学术

Analysis of clinical manifestations and treatment in 26 children with fibrodysplasia ossificans progressiva in China

Published:2019-09-16 Issue:1 Volume:16 Page:82-88
ISSN:1708-8569
Container-title:World Journal of Pediatrics
language:en
Short-container-title:World J Pediatr

Author:

Zhang Jun-Mei,Li Cai-Feng,Ke Shuang-Ying,Piao Yu-Rong,Han Tong-Xin,Kuang Wei-Ying,Wang Jiang,Deng Jiang-Hong,Tan Xiao-Hua,Li Chao

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12519-019-00302-x.pdf

Reference21 articles.

1. Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, et al. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet. 2006;38:525–7.

2. Alessi Wolken DM, Idone V, Hatsell SJ, Yu PB, Economides AN. The obligatory role of activin A in the formation of heterotopic bone in fibrodysplasia ossificans progressiva. Bone. 2018;109:210–7.

3. The medical management of fibrodysplasia ossificans progressive: current treatment considerations International Clinical Consortium on FOP: Philadelphia; 2019.

4. Illingworth RS. Myositis ossificans progressiva (Munchmeyer's disease). Brief review with report of two cases treated with corticosteroids and observed for 16 years. Arch Dis Child. 1971;46:264–8.

5. Bocciardi R, Bordo D, Di Duca M, Di Rocco M, Ravazzolo R. Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements. Eur J Hum Gent. 2009;17:311–8.

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