Literature DB >> 8958616

Fragile bone syndrome associated with craniognathic fibro-osseous lesions and abnormal modeling of the tubular bones: report of two cases and review of the literature.

G Nishimura1, N Haga, S Ikeuchi, T Yamaguchi, K Aoki, M Yamato.   

Abstract

OBJECTIVE: To report examples of disorders characterized by bone fragility, calvarial and/or gnathic fibro-osseous lesions, and metadiaphyseal undermodeling of the tubular bones.
DESIGN: The clinical, radiological, and pathological features of two patients are described and the literature reviewed. PATIENTS: The patients comprised a 10-year-old boy and a 48-year-old woman. The former exhibited multiple fractures starting in early childhood and calvarial masses which developed in late childhood; the latter showed a mandibular mass.
RESULTS: Calvarial doughnut lesions, osteopenia with coarse bony trabeculae, and undermodeling of the lower limbs were radiologically demonstrated in the first patient, while multiple sclerotic foci in the maxilla and mandible, spontaneous bowing of the right femur, and minimal undermodeling of the tibiae were demonstrated in the second. Bone biopsy of the iliac crest in the first patient revealed histologically normal bony trabeculae. Bone histomorphometry suggested an increased osteoid surface. Osteoid volume was also slightly increased. The pathological findings of the mass in the jaw in the latter patient were consistent with it being a fibro-osseous lesion. The literature review revealed several patients whose features overlapped with those of our patients.
CONCLUSION: These patients may represent a group of fragile bone syndromes which differ from osteogenesis imperfecta.

Entities:  

Mesh:

Year:  1996        PMID: 8958616     DOI: 10.1007/s002560050167

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  6 in total

Review 1.  Fibro-osseous lesions of the craniofacial skeleton: an update.

Authors:  Samir K El-Mofty
Journal:  Head Neck Pathol       Date:  2014-11-20

2.  Gnathodiaphyseal dysplasia: report of a family with a novel mutation of the ANO5 gene.

Authors:  Hannah A Duong; Karen T Le; Albert L Soulema; Ronald H Yueh; Maren T Scheuner; Michael F Holick; Russell Christensen; Tracey L Tajima; Angela M Leung; Sanjay M Mallya
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol       Date:  2016-01-28

3.  The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD).

Authors:  Satoshi Tsutsumi; Nobuyuki Kamata; Tamara J Vokes; Yutaka Maruoka; Koichi Nakakuki; Shoji Enomoto; Ken Omura; Teruo Amagasa; Masaru Nagayama; Fumiko Saito-Ohara; Johji Inazawa; Maki Moritani; Takashi Yamaoka; Hiroshi Inoue; Mitsuo Itakura
Journal:  Am J Hum Genet       Date:  2004-04-29       Impact factor: 11.025

4.  Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia.

Authors:  Lingling Jin; Yi Liu; Fanyue Sun; Michael T Collins; Keith Blackwell; Albert S Woo; Ernst J Reichenberger; Ying Hu
Journal:  Sci Rep       Date:  2017-02-08       Impact factor: 4.379

5.  Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2.

Authors:  Minna Pekkinen; Paulien A Terhal; Lorenzo D Botto; Petra Henning; Riikka E Mäkitie; Paul Roschger; Amrita Jain; Matthijs Kol; Matti A Kjellberg; Eleftherios P Paschalis; Koen van Gassen; Mary Murray; Pinar Bayrak-Toydemir; Maria K Magnusson; Judith Jans; Mehran Kausar; John C Carey; Pentti Somerharju; Ulf H Lerner; Vesa M Olkkonen; Klaus Klaushofer; Joost Cm Holthuis; Outi Mäkitie
Journal:  JCI Insight       Date:  2019-04-04

6.  Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran.

Authors:  Vahid Reza Yassaee; Arash Khojasteh; Farzad Hashemi-Gorji; Hossein Sadeghi; Hannaneh Safiaghdam; Reza Mirfakhraie
Journal:  Mol Genet Genomic Med       Date:  2022-06-27       Impact factor: 2.473

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.