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35 Possible Causes for Clitoromegaly, Fused Labia

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  • Ambiguous Genitalia

    labia that may look like a scrotum A lump of tissue within the fused labia that can be confused with testicles In genetic males (one X and one Y chromosome - 46XY): A small[] Because of clitoromegaly and scrotal-like hypertrophy of the labia majora, she had an endocrine evaluation the results of which were normal.[] However, there was no identifiable change in management of clitoromegaly and the numbers of clitoral reduction operations remained high.[]

  • Adrenogenital Syndrome

    Moreover, female neonates typically have ambiguous genitalia comprising an enlarged clitoris, partly fused labia majora, and a common urogenital sinus instead of separated[] Abstract For preservation of postoperative sensitivity of the glans clitoris, clitoroplasty for clitoromegaly due to adrenogenital syndrome is reported.[] A 23-year-old Japanese woman had her male-like musculature, hirsutism, the absence of breast development and marked clitoromegaly.[]

  • Virilization

    If the timing is right, the genitals are virilized with effects ranging from enlarged clitoris to the development of a complete phallus and the fusing of the labia.[] OBJECTIVE: To describe a rare case of 45,X Turner's syndrome with elevated T and clitoromegaly caused by ovarian hilus cell hyperplasia. DESIGN: Case report.[] We report a typical case that we found at cesarean section to be associated with a virilized infant who manifested clitoromegaly and labial fusion.[]

  • Fraser Syndrome

    The baby had malformed and low-set ears, wide nasal bridge, pseudo-hypertelorism, widely spaced nipples and fused labia with adhesion.[] […] of Fraser syndrome with bilateral cryptophthalmos and other common features of Fraser syndrome including syndactyly (hands and feet bilaterally), ambiguous genitalia with clitoromegaly[] Also, the labia (folds of skin on either side of the vagina) may be fused abnormally. There are no guidelines for prevention of Fraser Syndrome.[]

  • Vulvar Disorder

    labia, an absent or partially formed vagina, urethra located on the clitoris.[] Table 26.1 Ambiguous External Genitalia Clinical Presentation Diagnosis Etiology Clitoromegaly or variable phallus formation with ventral opening; variable labial formation[] Developmental disorders [ edit ] Septate vagina Vaginal opening extremely close to the urethra or anus An imperforate hymen Various stages of genital masculinization including fused[]

  • True Hermaphroditism

    The labia ("lips" or folds of skin of the external female genitals) fuse, and the clitoris enlarges to appear like a penis.[] The presenting symptoms were ambiguous genitalia (6 patients), isolated clitoromegaly (1 patient) and hypospadias (1 patient).[] The initial manifestations were ambiguous genitalia in 20 cases (two of them identified prenatally by ultrasound examination), isolated clitoromegaly in one, and penile hypospadias[]

  • Female Gonadal Dysgenesis

    Labioscrotal swellings fuse and enlarge to become scrotum.[] Here we describe a rare association of gonadal dysgenesis and clitoromegaly in a girl with AT.[] The degree of genital ambiguity varies along a spectrum, ranging from an almost female phenotype with clitoromegaly at one extreme to an almost male phenotype with isolated[]

  • Disorder of Sex Development

    (Grades 1-3) XX individuals with Congenital Adrenal Hyperplasia (C.A.H.) with extensively fused labia and a penile clitoris XY individuals with Hypospadias Persons with Klinefelter[] We identified a partial NR5A1 deletion affecting exons 2 and 3, leading to NR5A1 haploinsufficiency in 1 patient presenting with female external genitalia with clitoromegaly[] Her goal of appearing mainstream while publicly discussing fused labia and unusual gonads seems, at times, unattainable.[]

  • 46,XX Ovotesticular Disorder of Sex Development

    […] small labia: such findings should prompt investigation in order to rule out a possible DSD.[] […] lyase combined deficiency side chain cleavage deficiency Genitalia do no appear 100% normal bilateral nonpalpable gonads severe hypospadias, esp with nonpalpable gonads clitoromegaly[] Persistant Müllerian duct syndrome Kallman syndrome 17-beta reductase deficiency (XX or XY) 46,XY 3-beta-hydroxysteroid dehydrogenase deficiency (HSD deficiency) Aphallia Clitoromegaly[]

  • Androgen Insensitivity Syndrome

    In PAIS, there may be undescended testes , a small penis , placement of the urethal opening on the underside of the penis, an enlarged clitoris, or fused labia.[] The subtle effects of AR mutations present in a patient with micropenis, peno-scrotal hypospadias, infertility, clitoromegaly and posterior labial fusion.[] Partial AIS : In some forms of PAIS, patients have a female body, with slightly ambiguous female genitalia (an enlarged clitoris and partially fused labia), testes in the[]

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