Clitoral enlargement secondary to neurofibromatosis.
نویسندگان
چکیده
منابع مشابه
Clitoromegaly as first presentation of a neurocutaneous syndrome in a 3-year-old girl
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.
متن کاملNeurofibromatosis presenting as painless clitoromegaly.
Received June 2008 Accepted September 2008 INTRODUCTION Neurofibromatosis is an autosomal dominant progressive disorder with an incidence of approximately 1 in 3000 live births.(1) Its recognized features include hyperpigmented skin lesions (cafe-au-lait spots), neurofibromas, iris hamartomas, macrocephaly, central nervous system tumors, defects of the skull and facial bones, and vascular lesio...
متن کاملOrbit deformities in craniofacial neurofibromatosis type 1.
BACKGROUND AND PURPOSE The possible relationship of orbit deformities in neurofibromatosis type 1 (NF1) to plexiform neurofibromas (PNFs) have not been fully elucidated. Our purpose was to review orbital changes in patients with craniofacial NF1. METHODS We retrospectively reviewed CT and MR imaging abnormalities of the orbit in 31 patients (18 male, 13 female; mean age, 14 years; age range 1...
متن کاملClitorectomy for the Management of Os Clitoris in a Dog
Introduction Disorders of genital development occur in all species of mammals (Cribiu and Chaffaux, 1990; Passello-Legrand and Mowat, 2004; Weng et al., 2005). In female dogs, the clitoris develops from the genital tubercle, as the penis in the male. The enlargement or ossification of clitoris may be caused by an abnormality of chromosome differentiation, by exposure to androgens or progestins ...
متن کاملConcomitant composite adrenal pheochromocytoma, multiple gastric stromal tumours and pseudohermaphrodism in a patient with von Recklinghausen's disease
Although pheochromocytoma occurs in 1% of patients with von Recklinghausen's disease, composite tumors in this syndrome are much rarer, with isolated case reports in the literature. Most gastrointestinal stromal tumors (GISTs) are solitary and sporadic. Multiple GISTs however, are associated with clinical syndromes particularly von Recklinghausen's disease. We believe this is the first report o...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Clinical pediatrics
دوره 32 5 شماره
صفحات -
تاریخ انتشار 1993