Tehran University of Medical Sciences Case Reports in Clinical Practice 2538-2683 10 6 2026 06 03 280 284 EN Shivani Shukla Department of Endocrinology, People’s College of Medical Sciences, Bhopal, India. Nancy Garg Department of Endocrinology, People’s College of Medical Sciences, Bhopal, India. Apoorva Suran Department of Endocrinology, People’s College of Medical Sciences, Bhopal, India. Jaideep Khare Department of Endocrinology, People’s College of Medical Sciences, Bhopal, India. 2026 02 27 2026 04 26 Turner syndrome is a rare but not uncommon genetic syndrome due to partial or complete loss of X-chromosome in females. Various chromosome anomalies identified are 45X0, isochromosome Xq, ring X, deletion Xp, or an abnormal Y chromosome, most common being 45X0.Clinical features depends on the type of chromosome anomaly present while generally include short stature, primary amenorrhea, hypogonadism. Hereby, we report a case of 18 year old female with Mosaic turner syndrome who presented with clinical finding of short stature with primary amenorrhea with coarctation of aorta. Patient was managed with multi-disciplinary approach that include growth hormone replacement, puberty induction and planning for ductal stenting.  https://crcp.tums.ac.ir/index.php/crcp/article/view/1176 https://crcp.tums.ac.ir/index.php/crcp/article/download/1176/763