Analysis:

Of course.

What is congenital ovarian hypoplasia?

Congenital ovarian hypoplasia, also known as Turner syndrome, is a disease caused by congenital chromosomal abnormalities. The normal female chromosome is 46, XX. Turner syndrome can be diagnosed if the karyotype is 45, XO, that is, a sex chromosome X, or 46, XXP or 46, XX q or its chimera is missing. Because of the abnormal sex chromosome, the ovary can't grow and develop, so it is a kind of cord-like fibrous tissue, with no primordial follicles and no eggs. The clinical features are short stature, the adult height rarely exceeds 150cm, the hairline of the neck is low, even reaching the shoulders, and the neck is short and thick. More than half of the neck skin is slack, webbed from the mastoid behind the ear to the acromion, chest is broad and shield-shaped, elbows are everted, * * * migrates outward, congenital aortic valve stenosis, amenorrhea, undeveloped secondary sexual characteristics, high FSH in the body and extremely low estrogen.

Different types of chimeras, such as 45, XO/46, XX, 45, XO/47, XXX, etc. , closer to normal women than 45 and XO. A few patients sometimes have menstrual cramps, * * development, and even pregnancy, but they have a high abortion rate and stillbirth rate.

No treatment can promote ovarian development and restore the patient's reproductive function. The purpose of treatment is to promote the development of height, * * * * and reproductive organs.