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Relevant bibliographies by topics / Clitoromegaly

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Dissertations / Theses
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Academic literature on the topic 'Clitoromegaly'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 June 2025

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Journal articles on the topic "Clitoromegaly"

1

Sutphen, Rebecca, Enrique Galán-Goméz, and Boris G. Kousseff. "Clitoromegaly in neurofibromatosis." American Journal of Medical Genetics 55, no. 3 (1995): 325–30. http://dx.doi.org/10.1002/ajmg.1320550316.

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Ch'ng, Tong Wooi, and Vatcharapan Umpaichitra. "A Case of Unusual Clitoromegaly." Journal of Pediatric and Adolescent Gynecology 31, no. 5 (2018): 543–45. http://dx.doi.org/10.1016/j.jpag.2018.04.004.

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HADDAD, NADINE G., GAIL H. VANCE, ERICA A. EUGSTER, MARY M. DAVIS, and MARTIN KAEFER. "Turner Syndrome (45x) with Clitoromegaly." Journal of Urology 170, no. 4 Part 1 (2003): 1355–56. http://dx.doi.org/10.1097/01.ju.0000085983.81063.3f.

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4

Fedele, Luigi, Eleonora Fontana, Stefano Bianchi, Giada Frontino, and Nicola Berlanda. "An unusual case of clitoromegaly." European Journal of Obstetrics & Gynecology and Reproductive Biology 140, no. 2 (2008): 287–88. http://dx.doi.org/10.1016/j.ejogrb.2008.02.008.

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5

Yesodharan, Dhanya, Bindu Sudarsanan, Annie Jojo, et al. "Plexiform Neurofibroma of Clitoris." Journal of Pediatric Genetics 06, no. 04 (2017): 244–46. http://dx.doi.org/10.1055/s-0037-1602789.

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AbstractThe most frequent genital presentation of neurofibromatosis in females is clitoromegaly. We report a case of a 5-year-old girl with neurofibromatosis type 1 with clitoral plexiform neurofibromatosis. Clitoroplasty was done, and the histopathology confirmed the diagnosis. Though rare, plexiform neurofibroma of clitoris should always be considered as a differential diagnosis in children with clitoromegaly before embarking on detailed investigations.

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Mohammed Mbarouk, Fatuma Lijohi, AK Mteta, Samuel Kibona, and Emanuel Itambu. "Idiopathic clitoromegaly: Reduction clitoroplasty at Al-Rahma Hospital Zanzibar Tanzania: A case report and review of the literature." World Journal of Advanced Research and Reviews 11, no. 2 (2021): 276–79. http://dx.doi.org/10.30574/wjarr.2021.11.2.0361.

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We present a case of 5 years old female with of idiopathic clitoromegaly managed by reduction clitoroplasty, preserving the dorsal neurovascular bundle and extensive network of nerves around the corpora to the glans Clitoromegaly is an embarrassing condition causing psychological stress, requiring intervention. The goals of clitoroplasty are to achieve normal genital anatomy and to preserve tactile sensation with a satisfactory sexual response.

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Aggarwal, SatishKumar, Vivek Manchanda, and Nitin Pant. "Epidermoid cyst of clitoris mimicking clitoromegaly." Journal of Indian Association of Pediatric Surgeons 15, no. 1 (2010): 23. http://dx.doi.org/10.4103/0971-9261.69137.

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8

Rabley, Andrew, Christopher E. Bayne, Archana Shenoy, and Romano T. DeMarco. "Genital Neurofibromatosis Presenting as Painful Clitoromegaly." Urology 133 (November 2019): 219–21. http://dx.doi.org/10.1016/j.urology.2019.07.016.

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9

Chatterjee, Subir K., Amal Chakravorti, and Jahurul Haque. "Clitoromegaly, duplex urethra, and dysplastic vagina." Pediatric Surgery International 9, no. 5-6 (1994): 444–47. http://dx.doi.org/10.1007/bf01686033.

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Hiers, Paul S., Rita Tatiana Abi Younes, and Michael J. Haller. "Apparent Clitoromegaly in Healthy Female Newborn." Pediatrics in Review 42, Supplement 2 (2021): 173–76. http://dx.doi.org/10.1542/pir.2020-0043.

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Dissertations / Theses on the topic "Clitoromegaly"

1

Fernandez-Aristi, Augusto Rafael, Andre Alonso Taco-Masias, and Luis Montesinos-Baca. "Case report: Clitoromegaly as a consequence of Congenital Adrenal Hyperplasia. An accurate medical and surgical approach." Elsevier Inc, 2018. http://hdl.handle.net/10757/623064.

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We present a case of a woman with a history of Congenital Adrenal Hyperplasia (CAH) diagnosed at the age of 12, who was referred to our unit for surgical treatment. Despite the initial diagnosis was an indirect inguinal hernia, it was a misdiagnosis. Once in our service, this was corrected into clitoromegaly secondary to CAH. Physical examination and imaging test discarded other abnormalities, such as secondary effects androgenization. Regarding surgical treatment, the techniques used were Spencer and Allen combined with Kumar, which are the most used for clitoroplasty but also less used

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2

Cruz, João Eduardo Oliveira. "Quisto Epidermoide do Clitóris." Master's thesis, 2016. http://hdl.handle.net/10400.6/5368.

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Introdução A clitoromegalia é definida como um clitóris de índice clitorial maior que 35mm2, é rara (1) e pode ser congénita ou adquirida.(2)(3) Pode ter origem em diversos quistos,(1)(6)(7) incluindo o quisto epidermoide.(3)(4)(5) Este resulta da implantação de fragmentos da epiderme no interior da derme, pode ocorrer durante o desenvolvimento embrionário ou por indução traumática.(6) Esta implantação é mais frequentemente originada por trauma, mais precisamente pela mutilação genital feminina (MGF).(7) Objectivos - Reportar um caso clínico ocorrido no Centro Hospitalar Cova da Beira (CHCB);

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Books on the topic "Clitoromegaly"

1

Thomas, David F. M. Disorders of sex development. Edited by David F. M. Thomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0124.

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The aetiology of disorders of sex development (DSD) is multifactorial and includes chromosomal defects, developmental abnormalities of the gonads, and defects of hormonal synthesis and expression. Infants born with ambiguous genitalia require urgent investigation because of the risk of hyponatraemia associated with congenital adrenal hyperplasia (CAH) and to permit an informed decision on gender assignment. CAH is the commonest form of DSD, accounting for around 80% of all infants born with ambiguous genitalia. Despite controversy regarding timing and consent, feminizing genitoplasty in early

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Book chapters on the topic "Clitoromegaly"

1

Pal, Manidip. "Clitoromegaly." In Urogynecology and Pelvic Reconstructive Surgery. Jaypee Brothers Medical Publishers (P) Ltd., 2016. http://dx.doi.org/10.5005/jp/books/12783_53.

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2

"Clitoromegaly." In Clinical Protocols in Pediatric and Adolescent Gynecology. CRC Press, 2003. http://dx.doi.org/10.3109/9780203493397-10.

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Moura Fellow, V. O., L. C. Kaupert Fellow, L. G. Gomes, J. A. M. Marcondes, B. B. Mendonca, and T. A. S. S. Bachega. "The Presence of Clitoromegaly in Nonclassical Form of 21-Hydroxylase Deficiency Is Modulated by the CAG Polymorphic Tract of Androgen Receptor Gene." In The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego. Endocrine Society, 2010. http://dx.doi.org/10.1210/endo-meetings.2010.part2.p9.p2-408.

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Conference papers on the topic "Clitoromegaly"

1

Jethwani, Umesh, and Divya Jethwani. "Sertoli cell tumor of ovary: A rare case report." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685324.

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Introduction: Sertoli-Leydig cell tumor (SLCT) is a rare ovarian tumor, Constitute less than 0.5% of ovarian tumors. Most tumors are unilateral, confined to the ovaries. They are seen during the second and third decades of life. They are characterized by the presence of testicular structures that produce androgens. Patients have symptoms of virilization (depending on the quantity of androgen). Case Report: A 42-year-old woman presented Amenorrhea for 14 months. Change in her voice for 1 year and Excessive hair growth on her face, chest, and limbs for the last 2 months. She complained of vague

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