DOMINANT DEAFNESS-ONYCHODYSTROPHY SYNDROME IN A NEWBORN (CLINICAL CASE)
Autosomal dominant deafness onychodystrophy syndrome (DDOD - dominant deafness onychodystrophy syndrome) belongs to a group of rare multisystem genetic diseases. Typical symptoms are congenital sensorineural hearing loss, onychodystrophy, brachydactyly, and triphalangeal thumbs. The article presents a clinical case of DDOD in a child diagnosed during the neonatal period
Authors
- С.В. Голубева
- E. A. Degtyareva (ORCID: https://orcid.org/0000-0002-3219-2145)
- YU.I. LEMESHKO
- A.B. SUSHCHEVSKY
- M.M. CHEPRASOVA
- E.A. YEROMINA
- I.A. TALANOVA
Publication Details
- Journal
- MODERN PERINATAL MEDICAL TECHNOLOGIES IN SOLVING THE PROBLEM OF DEMOGRAPHIC SECURITY
- Published
- 2024-12-01
- DOI
- https://doi.org/10.63030/2307-4795/2024.17.g.01
- Primary Topic
- Biotin and Related Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00