نتایج جستجو برای: clitoromegaly
تعداد نتایج: 97 فیلتر نتایج به سال:
Congenital adrenal hyperplasia is generally associated with oligo-amenorrhea, and its presentation with polymenorrhagia is rare. Here we present a case of an Asian female who presented with polymenorrhagia since menarche, increased body hair growth and enlargement of clitoris for 7-8 years. Examination revealed a normal Body Mass Index, moderate hirsutism, Tanner 5 breasts and significant clito...
Neurofibromatosis type 1, also called Von Recklinghausen Disease is a genetic disorder characterized by the development of multiple benign tumors affecting skin and nervous system. It disease with prevalence one case in 3000 births. The cause VRD mutation [1-4]. In half all cases NF1, faulty gene passed from parent to their child. Clitoromegaly presenting childhood can be congenital or acquired...
rabson-mendenhall syndrome is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia, postprandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. herein, we described a 10- year-old girl with physical f...
Leydig cell tumor is a rare benign which belongs to the category of sex cord stromal tumors ovary. usually presents with androgenizing features like hirsutism, deepening voice, or clitoromegaly and are often suspected only if such symptoms present. can however be estrogenizing non-functional. We report an incidental finding in patient who underwent hysterectomy for postmenopausal bleeding.
A rare cause of clitoral hypertrophy in a child is neurofibromatosis type 1 (NF1). Although evaluation, including karyotype and hormonal studies, is necessary to exclude ambiguous genitalia, the diagnosis of neurofibromatosis as a possible cause of clitoromegaly may help avoid lengthy and sometimes invasive interventions.
A two-year-and-eight-month-old girl presented with clitoromegaly and short stature. Two cell lines, 45,X and 46,X,idic(Y)(q11.2), were observed. Cytogenetic and fluorescence in situ hybridisation investigations were carried out on her peripheral lymphocytes and gonadal cells, to determine the genotype-phenotype effect with respect to differential tissue distribution, effects of the sex determin...
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