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microtia

Wednesday 19 January 2005

Etiology (Exemples)

- trisomy 13
- trisomy 21
- Townes-Brocks syndrome
- germline mutations of HOXA2 in autosomal recessive microtia (18394579)

See also

- Ears

References

- Alasti F, Sadeghi A, Sanati MH, Farhadi M, Stollar E, Somers T, Van Camp G. A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family. Am J Hum Genet. 2008 Apr;82(4):982-91. PMID: 18394579