AbstractTurner syndrome is one of the commonest surviving abnormal cytogenetic disorders which is mostly identified at the time of puberty. The cytogenetic abnormality can be in form of classic monosomy X, structural abnormality of X chromosome or mosaicism. The phenotype can be modified in the presence of the chromosomal make-up of an individual. Here we report a series of patients having milder phenotype prompting us to be more vigilant in girls having short height and obtaining cytogenetic studies at the earliest.