Article
[Mosaic trisomy 18. Series of cases].
Archivos argentinos de pediatria - 1 Jun 2017
Cammarata-Scalisi Francisco, Lacruz-Rengel María A, Araque Dianora, Da Silva Gloria, Avendaño Andrea, Callea Michele, Stock Frances, Guerrero Yudith, Aguilar Eliomar, Lacruz María J, Sulbaran Jesús
Abstract excerpt
Trisomy 18 syndrome (T18) is a clinical and genetic disorder, which has a full extra chromosome 18 in each cell, variant that is called free trisomy. In addition, it can occur in partial and mosaic form. It is characterized by intrauterine growth restriction, psychomotor and mental retardation, characteristic craniofacial findings, congenital heart disease, hypoplastic pelvis, clenched hand and rocker-bottom...
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