Midro A T, Panasiuk B, Radwan J, Sipowicz I, Jaworowska B, Korsak E
Service de Génétique Clinique Académie de Médecine de Bialystok, Pologne.
J Gynecol Obstet Biol Reprod (Paris). 1990;19(7):811-6.
We studied 150 women with primary/secondary amenorrhea and/or oligomenorrhea; in 61 cases we found an abnormal karyotype (i.e. 40.7%): 51 cases in the first group of 110 patients with amenorrhea (i.e. 46%) and 10 cases in the second group of 40 patients with oligomenorrhea and/or secondary amenorrhea (i.e. 25%). The chromosome aberrations we found consisted in X aneuploidy, male karyotype and the different structural changes as mono- and dicentric X isochromosomes, dicentric, ring, deleted or inverted X chromosomes. Our results suggest a cytogenetic examination in patients with primary amenorrhea as well as in patients with oligomenorrhea and/or amenorrhea secundaria.
我们研究了150例原发性/继发性闭经和/或月经过少的女性;在61例患者中我们发现了异常核型(即40.7%):在第一组110例闭经患者中有51例(即46%),在第二组40例月经过少和/或继发性闭经患者中有10例(即25%)。我们发现的染色体畸变包括X非整倍体、男性核型以及不同的结构变化,如单中心和双中心X等臂染色体、双中心、环状、缺失或倒位的X染色体。我们的结果表明,对于原发性闭经患者以及月经过少和/或继发性闭经患者应进行细胞遗传学检查。