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Defining dysmorphic facial features in congenital Zika syndrome.

Cristiane Sá Roriz FontelesFrancisco César MonteiroRebeca Bastos VasconcelosAndré Jalles MonteiroCauby Maia Chaves JúniorFelipe Franco MarçalRenata Asfor Rocha Carvalho MartinsAna Lalessa Pereira de OliveiraGrisielle de Sá CavalcanteBianca Palhano ToscanoThayse Elaine Costa Figueiredo LopesFabio Wildson Gurgel CostaThyciana Rodrigues RibeiroIslane Maria Castro VerçosaAndré Luiz Santos PessoaLuciano Pamplona de Góes CavalcantiErlane Marques Ribeiro
Published in: American journal of medical genetics. Part A (2020)
Congenital Zika syndrome (CZS) constitutes a recently identified malformation caused by Zika virus infection during pregnancy. Limited data is available to date on the facial dysmorphic features of these patients. This study evaluated the facial dysmorphisms of children with CZS, compared with clinically healthy children, using clinical examination and standardized photographic images. Sixty-three children with CZS (9.70 ± 3.2 months-age), and 31 Controls (8.67 ± 6.2 months-age) joined the study. Seven out of 15 indices differed between groups: midfacial height (MFH)/horizontal facial reference (HFR) (p = .0003), interalar distance/HFR (p = .0027), nasal root depth/MFH (p = .0030), posterior nasal length/MFH (p = .0002), vertical position of the ear/MFH (p <.0001), ear length/MFH (p = .0005), chin height/total facial height (CH/TFH) (p <.0001). A CH/TFH of 0.229 showed 93.9% sensitivity and 80.6% specificity in diagnosing CZS. Children with CZS had broad, short faces, decreased intercanthal distance, short posterior nasal length, prominent nasal root, broad nasal wings, and high-set and long ears. Increased chin height index provided the most accurate diagnostic potential.
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