Literature DB >> 16012045

Craniometaphyseal dysplasia.

Young Ho Kim1, Dong Hwan Roh, Byung Yoon Choi, Seung-Ha Oh.   

Abstract

Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the importance of the early detection of accompanying lesions.

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Year:  2005        PMID: 16012045     DOI: 10.1080/00016480510028474

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  2 in total

1.  Novel ANKH mutation in a patient with sporadic craniometaphyseal dysplasia.

Authors:  Allison Zajac; Seung-Hak Baek; Imad Salhab; Melissa A Radecki; Sukwha Kim; Hakon Hakonarson; Hyun-Duck Nah
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

2.  An atypical case of craniometaphyseal dysplasia. Case report and surgical treatment.

Authors:  Giorgio Novelli; Emanuela Ardito; Fabio Mazzoleni; Alberto Bozzetti; Davide Sozzi
Journal:  Ann Stomatol (Roma)       Date:  2017-11-08
  2 in total

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