Cleidocranial Dysplasia Causing Respiratory Distress in Neonates: A Case Report and Literature Review
Cleidocranial dysplasia (CCD; OMIM 119600) is a rare autosomal dominant skeletal dysplasia, which is mainly characterized by persistently open or delayed closure of fontanelle, patent skull sutures, abnormal clavicles, pectus excavatum, short stature, supernumerary teeth, and sinus and middle ear in...
Main Authors: | Ru Xue, Guoqing Zhang, Xiafang Chen, Xiuxia Ye |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-09-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2021.696685/full |
Similar Items
-
Cleidocranial dysplasia: A family report
by: Chelvan H, et al.
Published: (2009-01-01) -
Cleidocranial dysplasia syndrome with epilepsy: a case report
by: Yimei Ma, et al.
Published: (2019-04-01) -
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia
by: Wei-De Lin, et al.
Published: (2011-01-01) -
Cleidocranial dysplasia: Report of 4 cases and review
by: Virender Gombra, et al.
Published: (2008-01-01) -
A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
by: Emine Çamtosun, et al.
Published: (2019-09-01)