Turner Syndrome - 45,X Karyotype (Monosomy X) 

Turner Syndrome (TS) is a genetic condition affecting about one in 2,500 live-born females. It occurs in females with one normal X chromosome and either a complete or partial absence of the second sex chromosome. First described by Dr. Henry Turner in 1938, the condition is known for its characteristic features such as short stature, gonadal failure, and various health issues including cardiac anomalies, autoimmune disorders, osteoporosis, and increased risk of type 2 diabetes.
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