Characterising the speech phenotype in individuals with craniofacial microsomia: a scoping review protocol
Introduction Asymmetric mandibular hypoplasia, microtia, tongue and laryngeal anomalies, and soft palate and facial nerve dysfunction are clinical features observed in children with craniofacial microsomia (CFM). Despite involvement of all these structures in hearing and speech, there is limited evi...
Saved in:
| Main Authors: | Sara Kinter, Katelyn Kotlarek, Anna Meehan, Carrie Heike |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMJ Publishing Group
2023-02-01
|
| Series: | BMJ Open |
| Online Access: | https://bmjopen.bmj.com/content/13/2/e069233.full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A critical analysis of the management of craniofacial microsomia
by: David John David AC
Published: (2018-03-01) -
P288: A review of phenotypic and genetic data in craniofacial microsomia cases from a multidisciplinary craniofacial clinic
by: Elizabeth Sellars, et al.
Published: (2025-01-01) -
Structural and functional changes in the oral microbiome of patients with craniofacial microsomia
by: Tianying Zang, et al.
Published: (2025-02-01) -
125. Addressing Facial Asymmetry and Craniofacial Microsomia For Gender-affirming Reconstruction
by: Kelly X. Huang, BS, et al.
Published: (2025-05-01) -
Introduction of the distance methods of genetic counseling for the parents of children with craniofacial microsomia. Determination of the frequency of inheritance of the shape of the auricle
by: O. Z. Topolnitskiy, et al.
Published: (2019-02-01)