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Nager syndrome is a rare, complex malformation syndrome, for which there is limited information on prenatal genetic testing. Clinical diagnosis of Nager syndrome, which can be caused by deletions encompassing SF3B4 gene, is possible prenatally. Prenatal chromosomal microarray can aid genotype-phenotype correlation in pregnancies with structural abnormalities seen on ultrasound. © 2020 The Authors. Clinical Case Reports published by John Wiley Sons Ltd.Squamous cell carcinoma arising in hidradenitis suppurativa (HS) is a rare albeit
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