Table 4 Common syndromes reported in microtia subject
From: Genotype-phenotype associations in microtia: a systematic review
SYNDROME | n | % |
|---|---|---|
All Syndromes Found | 1257 | 100.00% |
 Craniofacial Microsomia | 1191 | 94.75% |
 Treacher Collin Syndrome | 29 | 2.31% |
 Branchiootorenal Syndrome | 8 | 0.64% |
 OAVS | 9 | 0.72% |
 Goldenhar Syndrome | 5 | 0.40% |
 Meier Gorlin Syndrome | 2 | 0.16% |
 Mandibulofacial dysostosis with microcephaly Syndrome | 2 | 0.16% |
 Wolf-Hirschhorn Syndrome | 1 | 0.08% |
 Coffin-siris Syndrome | 1 | 0.08% |
 15q24 deletion Syndrome | 1 | 0.08% |
 Kalmann Syndrome | 1 | 0.08% |
 Fraser Syndrome | 1 | 0.08% |
 Cat Eye Syndrome | 1 | 0.08% |
 Beals Syndrome | 1 | 0.08% |
 trisomy 13 mosaicism | 1 | 0.08% |
 EVEN-PLUS | 3 | 0.24% |