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. Author manuscript; available in PMC: 2022 Oct 3.
Published in final edited form as: Cleft Palate Craniofac J. 2020 Aug 12;58(1):42–53. doi: 10.1177/1055665620947987

Table 1.

Participant characteristics

Characteristic Controls (n = 72) Cases (n = 89)
M SD M SD
Age at assessment (months) 38.6 2.0 38.1 1.8
Hollingshead Socioeconomic Status 38.3 14.5 35.8 13.7
N % N %

Sex
 Male 31 43.1 56 62.9
 Female 41 56.9 33 37.1
Race
 White 42 58.3 69 77.5
 Black/African American 4 5.6 1 1.1
 Asian 0 0.0 6 6.7
 American Indian/Alaskan Native 3 4.2 2 2.2
 Other race 4 5.6 2 2.2
 Multiracial 19 26.4 7 7.9
Ethnicity
 Hispanic/Latino 27 39.1 49 56.3
 Not Hispanic/Latino 42 60.9 38 43.7
Language
 English 56 77.8 60 67.4
 Spanish 6 8.3 7 7.9
 Combination English/Spanish 10 13.9 22 24.7
CBCL Respondent
 Mother 65 90.3 78 87.6
 Father 6 8.3 8 9.0
 Other 1 1.4 3 3.4
Phenotype (cases only)
 Microtia only - - 27 30.3
 Microtia with mandibular hypoplasia - - 46 51.7
 Other CFM-associated features - - 16 18.0
Hearing Loss
 None - - 16 18.0
 Unilateral - - 68 76.4
 Bilateral - - 5 5.6
Study Site
 Children’s Hospital Los Angeles 7 9.7 37 41.6
 Children’s Hospital of Philadelphia 5 6.9 1 1.1
 Seattle Children’s Hospital 48 66.7 29 32.6
 University of North Carolina, Chapel Hill 6 8.3 12 13.5
 University of Illinois, Chicago 6 8.3 10 11.2
Developmental Interventions
 Physical Therapy 1 1.4 9 10.1
 Occupational Therapy 4 5.6 8 9.0
 Developmental Services 2 2.8 10 11.2
 Speech, Language, or Hearing Services 7 9.7 61 68.5

Abbreviations: CBCL, Child Behavior Check List; CFM, craniofacial microsomia; SD, standard deviation