Agnathia Explained

Synonym:-->
Symptoms:Absence of a portion or the entirety of one or both jaws.
Cause:-->
Risk:-->
Diagnosis:X-rays or CT scans of the mandible and temporomandibular joint.
Treatment:Surgery
Frequency:Rare.
Eponym:-->

Agnathia (also termed hypognathous) is the absence of a portion or the entirety of one or both jaws.[1] [2] It is a very rare condition. External, middle, and inner ear abnormalities, as well as temporal bone, parotid gland, masticatory muscles, and facial neural abnormalities, frequently coexist with Agnathia. Agnathia is seen in agnathia-holoprosencephaly, otocephaly, and Ivemark syndrome.[3]

Diagnosis

X-rays or CT scans of the mandible and temporomandibular joint showcase the extent of underdevelopment and differentiate Agnathia from other disorders that cause similar facial abnormalities but do not involve substantial structural loss.[3]

Treatment

Agnathia treatment consists of rapid reconstruction using autogenous bone grafting to stop the further development of facial deformity. Mentoplasty, bone and cartilage onlay grafts, and soft-tissue grafts are frequently used to restore facial symmetry. Distraction osteogenesis, which involves performing an osteotomy and attaching a distraction device to both portions of the mandible, is becoming more common. Early orthodontic therapy in adolescents aids in the correction of malocclusion.[3]

See also

Notes and References

  1. Book: Ghom AG. Ghom SA. Textbook of Oral Medicine. 30 September 2014. JP Medical Ltd. 978-93-5152-303-1. 125.
  2. Book: Rajendran A. Sundaram S. Shafer's Textbook of Oral Pathology. 7th. 10 February 2014. Elsevier Health Sciences APAC. 978-81-312-3800-4. 12.
  3. Web site: 2023-09-29. Congenital Jaw Abnormalities - Pediatrics. Merck Manuals Professional Edition.