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Aglossia

Congenital tongue disorder

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionSep 21, 2026
Entity authorityQ9588048
Source-derived summary

Aglossia (aglossia congenita) is defined as the substantial loss of tongue. Instances of isolated aglossia (as in aglossia on its own without any other congenital limb defects) are exceedingly rare.

Severity

Aglossia is the most severe form of tongue size defects. It is more severe than other related conditions like hypoglossia, microglossia, and macroglossia.

Unlike aglossia, individuals with hypoglossia/microglossia have a tongue, but the length and width of their tongue is shorter than average. Macroglossia on the other hand refers to tongues that are abnormally large.

Associations with other conditions

Oftentimes, aglossia is associated with other congenital conditions. One example is aglossia-adactylia, characterized as aglossia with digital malformations.

Aglossia can also be associated with defects in other regions of the body, such as the cranium, face, mouth, teeth, cardiovascular system, central nervous system, as well as other internal organs.

Aglossia is also seen as a symptom of a broader set of oromandibular limb hypogenesis syndrome (OLHS) conditions, such as Moebius syndrome and Hanhart syndrome.

Editorial summary

Begin with the source’s own compact description: “Aglossia” is congenital tongue disorder. The dossier treats that line as a proposition to test through Aglossia, Congenital and tongue, not as a finished interpretation.

Editorial reviewA dependable orientation record for establishing vocabulary, names and a first evidence trail. The current 164-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. For this dossier, Aglossia, Congenital and tongue is the immediate research focus.
Editorial analysis

Why this record matters

The phrase “congenital tongue disorder” supplies a clear boundary for inquiry. It also exposes the unanswered questions: who defined that boundary, when it became stable and which sources sit outside it.

Evidence profile

The citation trail is more important than the brevity of the summary: it shows where individual claims can be examined in context. The source revision retrieved here is dated Sep 21, 2026. The linked authority identifier is Q9588048. None of the 0 selected statements returned an explicit reference.

Critical limits

The absence of detail may reflect summary conventions rather than a lack of surviving documentation. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

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Source & attribution

This entry incorporates text from Aglossia” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.