Cleidocranial dysplasia—Review with an emphasis on otological and audiological manifestations

Author:

Segal Nili,Puterman Moshe

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. Cleidocranial dysplasia: clinical and molecular genetics;Mundlos;Med. Genet.,1999

2. Sur la dysostose cleido-cranienne hereditaire;Marie;Rev. Neurol.,1989

3. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia;Mundlos;Cell,1997

4. CBFA1 a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development;Otto;Cell,1997

5. CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia;Zhou;Hum. Mol. Genet.,1999

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1. Best practice guidelines in managing the craniofacial aspects of skeletal dysplasia;Orphanet Journal of Rare Diseases;2021-01-14

2. Cleidocranial Dysplasia;Journal of Craniofacial Surgery;2020-06

3. Audiological evaluation of patients with cleidocranial dysplasia (CCD);EUR REV MED PHARMACO;2020

4. Cleidocranial dysplasia-dental disorder treatment and audiology diagnosis;Open Medicine;2018-01-01

5. Cleidocranial Dysplasia;Atlas of Genetic Diagnosis and Counseling;2017

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