Hypogonadotropic hypogonadism: Can have multiple pregnancy and or ovarian hyper stimulation syndrome
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چکیده
منابع مشابه
Behçet Syndrome and Hypogonadotropic Hypogonadism: case report
Clinical case A sixteen year old boy presented, three years before, gastrointestinal (abdominal pain, vomiting, diarrhea) and neurologic symptoms (headache, diplopia, ataxia, VI nerve paralysis), with fever, oral and genital aphtosis. Laboratory tests showed increased ESR, CRP). He carried B51HLA. Physical examination showed svere obesity, pseudomicropenis, rare pubic hair, pubertal stage G2P2....
متن کاملI-3: Hypogonadotropic Hypogonadism
Hypogonadotropic hypogonadism (HH) is an uncommon cause of male infertility and a congenital or secondary disorder characterized by delayed or absent sexual maturation. Congenital abnormalities leading to HH are usually the consequence of deficient GnRH secretion occurring either in isolation (idiopathic hypogonadotropic hypogonadism (IHH)), or in association with anosmia (Kallmann syndrome; KS...
متن کاملMoebius syndrome in association with hypogonadotropic hypogonadism.
The association between hypogonadotropic hypogonadism and multiple CNS lesions in a variety of disorders suggests a possible causative link between these clinical findings. Neural afferent input into the hypothalamus from higher CNS centers modulates GnRH secretion and derangements of these neural pathways could potentially result in diminished gonadotropin secretion and hypogonadism. This repo...
متن کاملovarian hyper stimulation syndrome in two spontaneous pregnancies
discussion the presence of ohss in spontaneous pregnancy especially in familial pattern may lead us to evaluate some endogenous pathogenic factors. case presentation in this case report, we are going to present two cases of ohss occurring in spontaneously conceived pregnancies. one of the patients mentioned the history of this syndrome in her sister, and the other one confronted with this syndr...
متن کاملCongenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future
The proper development and coordination of the hypothalamic-pituitary-gonadal (HPG) axis are essential for normal reproductive competence. The key factor that regulates the function of the HPG axis is gonadotrophin-releasing hormone (GnRH). Timely release of GnRH is critical for the onset of puberty and subsequent sexual maturation. Misregulation in this system can result in delayed or absent p...
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ژورنال
عنوان ژورنال: Clinical Obstetrics, Gynecology and Reproductive Medicine
سال: 2019
ISSN: 2059-4828
DOI: 10.15761/cogrm.1000252