Literature DB >> 35527416

[Clinical features and FGFR3 mutations of children with achondroplasia].

Hui-Qin Zhang1, Dong-Ying Tao1, Jing-Jing Zhang1, Huan-Hong Niu1, Jian-Feng Luo1, Sheng-Quan Cheng1.   

Abstract

OBJECTIVES: To study the clinical features and fibroblast growth factor receptor 3 (FGFR3) gene mutations of children with achondroplasia (ACH) through an analysis of 17 cases.
METHODS: A retrospective analysis was performed on the clinical data and FGFR3 gene detection results of 17 children with ACH who were diagnosed from January 2009 to October 2021.
RESULTS: Of the 17 children with ACH, common clinical manifestations included disproportionate short stature (100%, 17/17), macrocephaly (100%, 17/17), trident hand (82%, 14/17), and genu varum (88%, 15/17). The common imaging findings were rhizomelic shortening of the long bones (100%, 17/17) and narrowing of the lumbar intervertebral space (88%, 15/17). Major complications included skeletal dysplasia (100%, 17/17), middle ear dysfunction (82%, 14/17), motor/language developmental delay (88%, 15/17), chronic pain (59%, 10/17), sleep apnea (53%, 9/17), obesity (41%, 7/17), foramen magnum stenosis (35%, 6/17), and hydrocephalus (24%, 4/17). All 17 children (100%) had FGFR3 mutations, among whom 13 had c.1138G>A hotspot mutations of the FGFR3 gene, 2 had c.1138G>C mutations of the FGFR3 gene, and 2 had unreported mutations, with c.1252C>T mutations of the FGFR3 gene in one child and c.445+2_445+5delTAGG mutations of the FGFR3 gene in the other child.
CONCLUSIONS: This study identifies the unreported mutation sites of the FGFR3 gene, which extends the gene mutation spectrum of ACH. ACH is a progressive disease requiring lifelong management through multidisciplinary collaboration.

Entities:  

Keywords:  Achondroplasia; Child; Fibroblast growth factor receptor 3 gene; Gene mutation

Mesh:

Substances:

Year:  2022        PMID: 35527416      PMCID: PMC9044984          DOI: 10.7499/j.issn.1008-8830.2111039

Source DB:  PubMed          Journal:  Zhongguo Dang Dai Er Ke Za Zhi        ISSN: 1008-8830


  29 in total

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2.  Hearing loss in skeletal dysplasia patients.

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Review 3.  Achondroplasia: Development, pathogenesis, and therapy.

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Journal:  Dev Dyn       Date:  2017-03-02       Impact factor: 3.780

4.  Epidemiology of achondroplasia: A population-based study in Europe.

Authors:  Alessio Coi; Michele Santoro; Ester Garne; Anna Pierini; Marie-Claude Addor; Jean-Luc Alessandri; Jorieke E H Bergman; Fabrizio Bianchi; Ljubica Boban; Paula Braz; Clara Cavero-Carbonell; Miriam Gatt; Martin Haeusler; Kari Klungsøyr; Jennifer J Kurinczuk; Monica Lanzoni; Nathalie Lelong; Karen Luyt; Olatz Mokoroa; Carmel Mullaney; Vera Nelen; Amanda J Neville; Mary T O'Mahony; Isabelle Perthus; Judith Rankin; Anke Rissmann; Florence Rouget; Bruno Schaub; David Tucker; Diana Wellesley; Katarzyna Wisniewska; Nataliia Zymak-Zakutnia; Ingeborg Barišić
Journal:  Am J Med Genet A       Date:  2019-07-11       Impact factor: 2.802

Review 5.  Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history.

Authors:  Julie Hoover-Fong; Moira S Cheung; Virginia Fano; Lars Hagenas; Jacqueline T Hecht; Penny Ireland; Melita Irving; Klaus Mohnike; Amaka C Offiah; Ericka Okenfuss; Keiichi Ozono; Cathleen Raggio; Louise Tofts; Dominique Kelly; Renée Shediac; Wayne Pan; Ravi Savarirayan
Journal:  Bone       Date:  2021-02-03       Impact factor: 4.398

6.  Factors associated with health-related quality of life (HRQOL) in adults with short stature skeletal dysplasias.

Authors:  Nitasha Dhiman; Alia Albaghdadi; Cheryl K Zogg; Meesha Sharma; Julie E Hoover-Fong; Michael C Ain; Adil H Haider
Journal:  Qual Life Res       Date:  2016-11-19       Impact factor: 4.147

7.  Sleep-disordered breathing and its management in children with achondroplasia.

Authors:  Rossana Tenconi; Sonia Khirani; Alessandro Amaddeo; Caroline Michot; Geneviève Baujat; Vincent Couloigner; Livio De Sanctis; Syril James; Michel Zerah; Valérie Cormier-Daire; Brigitte Fauroux
Journal:  Am J Med Genet A       Date:  2017-02-27       Impact factor: 2.802

8.  Natural history of achondroplasia: A retrospective review of longitudinal clinical data.

Authors:  Ericka Okenfuss; Billur Moghaddam; Andrew L Avins
Journal:  Am J Med Genet A       Date:  2020-08-31       Impact factor: 2.802

9.  High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study.

Authors:  Svein O Fredwall; Unni Steen; Olga de Vries; Cecilie F Rustad; Heidi Beate Eggesbø; Harald Weedon-Fekjær; Ingeborg B Lidal; Ravi Savarirayan; Grethe Månum
Journal:  Orphanet J Rare Dis       Date:  2020-05-25       Impact factor: 4.123

10.  Natural history of 39 patients with Achondroplasia.

Authors:  Jose Ricardo Magliocco Ceroni; Diogo Cordeiro de Queiroz Soares; Larissa de Cássia Testai; Rachel Sayuri Honjo Kawahira; Guilherme Lopes Yamamoto; Sofia Mizuho Miura Sugayama; Luiz Antonio Nunes de Oliveira; Debora Romeo Bertola; Chong Ae Kim
Journal:  Clinics (Sao Paulo)       Date:  2018-07-02       Impact factor: 2.365

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