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Copyright © 2020 by The American Association of Immunologists, Inc.The advance in the human genetic field has permitted to identify small chromosome alterations and associate them to a specific phenotype. However, there are many mutations that have not yet been described in the literature. We describe the clinical case of a term newborn with appropriate weight to its gestational age, without perinatal background of interest that, at birth, presented macrocephaly, hypertelorism, low-set ears, prominent forehead, micrognathia, camptodactyly
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