Developmental stuttering with common and complex phenotypes
Phenotypic analysis of a large cohort of who stutter identified 90% with a common phenotype and 10% with a complex phenotype. Both had co-occurring disorders requiring multidisciplinary support.
Authors
- Miya St John (ORCID: https://orcid.org/0000-0003-4723-937X)
- Daisy A. Shepherd (ORCID: https://orcid.org/0000-0001-8540-0473)
- Juliette Catherall
- Stephanie Siemers
- Angela T Morgan
- Sarah E Horton
- Ingrid E Scheffer
Institutions
- Royal Children's Hospital (AU)
- The University of Melbourne (AU)
- Florey Institute of Neuroscience and Mental Health (AU)
- Murdoch Children's Research Institute (AU)
- Austin Health (AU)
Publication Details
- Journal
- Developmental Medicine & Child Neurology
- Published
- 2026-02-23
- DOI
- https://doi.org/10.1111/dmcn.70208
- Primary Topic
- Stuttering Research and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00