Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstruction
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference13 articles.
1. Craniometaphyseal dysplasia — variability of expression within a large family;Beighton;Clin. Gen.,1979
2. Autosomal dominant craniometaphyseal dysplasia: clinical variability;Carnevale;Clin. Genet.,1983
3. A new look at craniometaphyseal dysplasia;Cole;J. Pediatr.,1988
4. Craniometaphyseal dysplasia with increased bone turnover and secondary hyperparathyroidism: therapeutic effect of calcitonin;Fanconi;J. Pediatr.,1988
5. Syndromes of the Head and Neck;Gorlin,1990
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1. Three-dimensional radiographic features of craniometaphyseal dysplasia—a comparative CBCT study;Journal of Rare Diseases;2023-04-03
2. Turbinoplasty surgery for nasal obstruction in craniometaphyseal dysplasia: A case report and review of the literature;International Journal of Pediatric Otorhinolaryngology;2015-06
3. Infant With Persistent Nasal Obstruction;JAMA Otolaryngology–Head & Neck Surgery;2014-10-01
4. Dental Anomalies Associated with Craniometaphyseal Dysplasia;Journal of Dental Research;2014-03-24
5. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD);Human Molecular Genetics;2010-12-13
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