What Are the Most Common Turner Syndrome Symptoms?

Turner syndrome is a rare chromosomal abnormality characterized by a complete or partial X chromosome monomer. The single X chromosome comes from the mother, and the missing X chromosome is caused by the non-separation of the sex chromosome of the father's spermatocyte. The clinical manifestations are short genitalia, genital and secondary sexual characteristics, and abnormal development of a group of bodies. Laboratory diagnosis can provide the basis for clinical diagnosis of Turner syndrome through laboratory inspection methods such as chromosome inspection and molecular genetics inspection.