Tasdemir, PelinZamani, Ayse GulDemirel, Sennur S.Acar, Aynur2020-03-262020-03-2620121895-1058https://dx.doi.org/10.2478/s11536-011-0162-6https://hdl.handle.net/20.500.12395/27918Distal trisomy 10q is a well delineated but a rare syndrome with characteristic phenotypic features. We present clinical and cytogenetic data on a 7 day-old girl with distal 10q trisomy (10q24 -> qter), due to maternal t(10.22) reciprocal translocation. Her karyotype showed an unbalanced translocation between chromosomes 10 and 22, resulting in trisomy of the distal part of the long arm of chromosome 10q24.en10.2478/s11536-011-0162-6info:eu-repo/semantics/openAccessDistal trisomy 10qFacial dysmorphismCongenital malformationsFamilial reciprocal translocationsDistal trisomy 10q24 due to maternal 10;22 translocation, third case in the same familyArticle73366370N/AWOS:000304396200018Q4