X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4
X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4
About this item
Full title
Author / Creator
Publisher
United States: American Speech-Language-Hearing Association
Journal title
Language
English
Formats
Publication information
Publisher
United States: American Speech-Language-Hearing Association
Subjects
More information
Scope and Contents
Contents
The authors report on a 7-year-old male, designated FR, who has severe sensorineural hearing loss. Features include a round face, hypertelorism, epicanthal folds, and flat nasal root. Although there were early developmental concerns regarding FR, all but his speech delay resolved when he was placed in an educational program that accommodated his he...
Alternative Titles
Full title
X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4644427
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4644427
Other Identifiers
ISSN
1059-0889
E-ISSN
1558-9137
DOI
10.1044/1059-0889(2013/13-0018)
