Women's and Newborn Services, Royal Brisbane and Woman's Hospital, Herston, Queensland, Australia.
Queensland Statewide Paediatric and Adolescent Gynaecology Service, Queensland Children's Hospital, South Brisbane, Queensland, Australia
BMJ Case Rep. 2021 Apr 9;14(4):e239495. doi: 10.1136/bcr-2020-239495.
Idiopathic hypogonadotropic hypogonadism (IHH) refers to a family of genetic disorders that affect the production and/or action of gonadotropic-releasing hormone, resulting in reduced serum levels of sex steroids. This condition has a prevalence of 1-10 cases/100 000 births and is characterised by the absence of spontaneous pubertal development. In women, the condition is characterised by the onset of normal adrenarche, with the absence of thelarche and menarche. Pubertal induction for breast development and uterine growth with oestradiol, and sequential maintenance of a normal menstrual cycle and adequate oestrogen for bone health, with an oestrogen and progesterone, is considered first-line treatment. Pregnancy can be achieved in patients who have received and responded to treatment with ovulation induction with exogenous gonadotrophins. Advances in genetic testing have led to increased research and understanding of the underlying genetics of IHH with gene mutations described in up to 50% of all IHH cases.
特发性低促性腺激素性性腺功能减退症(IHH)是一组遗传性疾病,影响促性腺激素释放激素的产生和/或作用,导致血清性激素水平降低。这种疾病的发病率为 1-10 例/100000 例出生,其特征是自发青春期发育缺失。在女性中,该疾病的特征是正常肾上腺功能初现,而乳房发育和初潮缺失。使用雌二醇诱导乳房发育和子宫生长,并序贯维持正常月经周期和足够的雌激素以促进骨骼健康,使用雌激素和孕激素,被认为是一线治疗方法。接受外源性促性腺激素诱导排卵治疗并对其有反应的患者可以实现妊娠。遗传检测的进步导致对 IHH 潜在遗传学的研究和理解增加,多达 50%的 IHH 病例描述了基因突变。