Aglossia
| Aglossia | |
|---|---|
| Symptoms | Partial or complete absence of tongue[1] |
| Usual onset | At birth[1] |
| Frequency | Rare[1] |
Aglossia (aglossia congenita) is a congenital defect resulting in a partial development or complete absence of a tongue.[1] It is typically associated with characteristic facial features such as a small chin.[1]
The first known case was reported in the early 18th century by a member of the prominent De Jussieu family in France and cases to this day remain rare.[2]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 "Orphanet: Isolated congenital hypoglossia/aglossia". www.orpha.net. Archived from the original on 5 June 2024. Retrieved 19 October 2025.
- ↑ Gupta, SR (2012). "Isolated aglossia congenita: A rare case of oromandibular limb hypogenesis syndrome type I B". J Oral Maxillofac Pathol. 16 (3): 414–9. doi:10.4103/0973-029X.102504. PMC 3519220. PMID 23248477.