287 Cases of amenorrhea in patients with cytogenetic.docVIP

 PAGE \* MERGEFORMAT 9 287 Cases of amenorrhea in patients with cytogenetic Of: Yu Xiaoyan Huang Yinghao Songjie Ping Pan Guying [Keywords:] Cytogenetic Analysis of amenorrhea Amenorrhea is a common symptom of gynecological diseases [1], usually divided into primary and secondary 2. Primary amenorrhea is more rare, often because of genetic or congenital developmental defects caused by reasons, the main pipe hypoplasia Miller syndrome, gonadal dysgenesis, confrontational ovary syndrome, androgen insensitivity syndrome, and low gonadotropin hypogonadism. which gonadal dysgenesis, including Turner’s syndrome, 46, XX and Article 46, XY cords gonadal dysgenesis. secondary amenorrhea genetic reasons cause premature ovarian failure, polycystic ovary syndrome, and external factors. In order to investigate the influence of genetic factors on menopause, this paper carried out on 287 cases of amenorrhea genetic analysis, combined with clinical performance studies, reports are summarized below. Subjects and methods 1. Target: January 1995 to June 2008 to Xiaogan Central Hospital and the Provincial Women and Children genetic counseling clinic’s 287 patients with amenorrhea and menstrual thinning hair, including 157 cases of primary amenorrhea, secondary amenorrhea and 96 cases 34 cases of patients with menstrual thin hair, aged between 13 to 38 years. 2. Asked about the history and relevant examination: to understand the childhood growth and development, with or without birth defects or other diseases and family history. Detail about menstrual history and other factors; check the general development of the situation, internal and external genital development, with or without congenital defects, deformities, inguinal lumps, distribution of secondary sexual characteristics such as hair, breast development is normal, whether breast milk secretion. reproductive organ abnormalities of suspected patients with B-ultrasound ovarian, uterine shape and location. all