Micrognathism

Micrognathism
Classification and external resources
ICD-10	K07.0
ICD-9	524.04
DiseasesDB	22641
MedlinePlus	003306
MeSH	D008844

Micrognathism (or Micrognathia) is a condition where the jaw is undersized. It is also sometimes called "Mandibular hypoplasia".^{[citation needed]} It is common in infants, but is usually self-corrected during growth, due to the jaws increasing in size. It may be a cause of abnormal tooth alignment and in severe cases can hamper feeding.^{[citation needed]}

Causes

While not always pathological, it can present as a birth defect in multiple syndromes including: fetal alcohol syndrome, congenital rubella, DiGeorge's Syndrome, Ehlers-Danlos Syndrome, Pierre Robin syndrome, Hallermann-Streiff syndrome, Trisomy 13(Patau syndrome), Trisomy 18 (Edwards syndrome), X0 syndrome (Turner syndrome), Progeria, Treacher Collins syndrome, Smith-Lemli-Opitz syndrome, Russell-Silver syndrome, Seckel syndrome, Juvenile idiopathic arthritis, Cri du chat syndrome, Bloom syndrome and Marfan syndrome.

Diagnosis

It can be detected by the naked eye as well as dental or skull X-Ray testing

See also

• Human mandible

References

• "Micrognathia". Medline Plus. 12 May 2009. http://www.nlm.nih.gov/medlineplus/ency/article/003306.htm. Retrieved 21 May 2011.