Aglossia

From Wikipedia, the free encyclopedia

Aglossia (aglossia congenita) is a congenital defect resulting in a partial development or complete absence of a tongue.

Aglossia is commonly associated with craniofacial and limb defects () and is thought to belong to a family of (OLHS). It is believed to be caused by heat-induced vascular disruption near the fourth week of embryonic development.

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.[1]

References[]

  1. ^ Gupta, SR (2012). "Isolated aglossia congenita: A rare case of oromandibular limb hypogenesis syndrome type I B". J Oral Maxillofac Pathol. 16: 414–9. doi:10.4103/0973-029X.102504. PMC 3519220. PMID 23248477.

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