Case of post‐orgasmic illness syndrome associated with hypogonadism
نویسندگان
چکیده
منابع مشابه
Postorgasmic illness syndrome: semen allergy in men.
Natural reproduction is an interaction process between gametes, female (oocyte) and male (spermatozoon), that occurs after spermatozoon travel along reproductive sexual tract during which it suffers several physiological and biochemical changes called capacitation. After capacitation, the spermatozoa are capable of undergoing acrosome reaction upon stimulation by the pellucid zone. In humans du...
متن کاملa case of primary hypogonadism with features of albright’s syndrome
background: mccune albright syndrome is rare with an estimated prevalence of 1 in 100,000 to 1 in 1,000,000 persons. the classical clinical triad consists of fibrous dysplasia of the bone, café-au-lait skin spots and precocious puberty. however, in rare cases, there may be primary hypogonadism and amenorrhea. case presentation: an eighteen-year-old female presented with amenorrhea. she had a sh...
متن کاملA Case of Primary Hypogonadism with Features of Albright’s Syndrome
BACKGROUND McCune Albright syndrome is rare with an estimated prevalence of 1 in 100,000 to 1 in 1,000,000 persons. The classical clinical triad consists of fibrous dysplasia of the bone, café-au-lait skin spots and precocious puberty. However, in rare cases, there may be primary hypogonadism and amenorrhea. CASE PRESENTATION An eighteen-year-old female presented with amenorrhea. She had a sh...
متن کاملBehçet 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 کاملReport of a case of Klippel-Trenaunay syndrome associated with bilateral nevus of Ota
Port-wine stain is a vascular malformation characterized pathologically by ectasia of superficial dermal capillaris and clinically by persistent macular erythema. The association of a port-wine stain on a limb with soft tissue swelling, with or without bony overgrowth, is termed klippel-Trenaunay syndrome. Phakomatosis pigmento-vascularis is a combination of port-wine stain and cutaneous ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: IJU Case Reports
سال: 2020
ISSN: 2577-171X,2577-171X
DOI: 10.1002/iju5.12184