Results 31 to 40 of about 2,537 (222)

Clitoromegaly in Premature Infants: Is It Truly Pathologic? [PDF]

Academic Journal of Pediatrics & Neonatology, 2021
Meenal Gupta
openaire   +2 more sources

Leydig tumor in normal sized ovaries causing clitoromegaly: A case report. [PDF]

Gynecol Oncol Rep
Chavez TF, Singh M, Avadhani V, Leonis R.   +3 more
europepmc   +2 more sources

Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy

JCRPE, 2023
Clitoromegaly usually develops due to hyperandrogenism. There are a few cases of clitoromegaly described without clinical and biochemical hyperandrogenism.
Büşra Gürpınar Tosun, Ahsen Karagözlü Akgül, Eda Almus, Sadık Abidoğlu, Serap Turan, Abdullah Bereket, Tülay Güran   +6 more
doaj   +1 more source

NERVE SPARING VENTRAL CLITOROPLASTY : A NEW TREATMENT FOR CLITOROMEGALY

Journal of Evolution of Medical and Dental Sciences, 2015
Immadi Chandra Sekhar, Vanaja G
openaire   +2 more sources

Clitoromegaly due to an epidermal inclusion cyst: A case report

Case Reports in Women's Health, 2022
Background: Clitoromegaly is often a sign of androgen excess; however, non-hormonal causes must be ruled out. We report the case of an adolescent with isolated clitoromegaly without clinical or biochemical evidence of hyperandrogenism.
Carolina Fux-Otta, Margarita Fuster, Noelia Ramos, Cristina Trezza, Mónica Ñañez, Ismael Fonseca, Néstor Dicuatro, Mariana Di Carlo, Carla Bongiorni, José Ochoa, Otilio Rosato, Peter Chedraui   +11 more
doaj   +1 more source

The spectrum of CYP21A2 gene mutations from 16 families of congenital adrenal hyperplasia: Genotype-phenotype correlation

Indian Journal of Endocrinology and Metabolism, 2021
Aim: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder of the adrenal steroidogenic pathway. The most common form of CAH is due to 21-hydroxylase deficiency resulting from mutations in CYP21A2 gene.
Subbiah Sridhar, Ramajayam Govindhan, Balasankar Soundian, Maheshkumar Poomarimuthu, Karuppasamy Nallan, Santhanakrishnan Ramesh kumar, Subbiah Eagappan, Vasanthiy Natarajan, Sangumani Jayaraman   +8 more
doaj   +1 more source

Functional characterisation of novel NR5A1 variants reveals multiple complex roles in Disorders of Sex Development [PDF]

, 2017
Variants in the NR5A1 gene encoding SF1 have been described in a diverse spectrum of disorders of sex development (DSD). Recently, we reported the use of a targeted gene panel for DSD where we identified 15 individuals with a variant in NR5A1, nine of ...
Ayers, K.L. (Katie L.), Baxendale, A. (Anne), Den Bergen, J.A. (Jocelyn A.), Eggers, S. (Stefanie), Faradz, S.M.H. (Sultana), Hanna, C. (Chloe), Hersmus, R. (Remko), Lafferty, A.R. (Antony R.), Listyasari, N.A. (Nurin A.), Looijenga, L.H.J. (Leendert), Marzuki, N.S. (Nanis S.), Ohnesorg, T. (Thomas), Riedl, S. (Stefan), Robevska, G. (Gorjana), Santosa, A., Sinclair, A. (Andrew), Thompson, E.M. (Elizabeth M.), Verge, C.F. (Charles F.), Warne, G. (Garry)   +18 more
core   +11 more sources

Clitoral preputial edema can be mistaken for clitoromegaly: a clinical analysis of ten cases

Frontiers in Endocrinology, 2023
Background and objectivesWe herein reported ten, female neonates with transient clitoral preputial edema, which was mistaken for clitoromegaly. Although it is well known that the clitoris is prominent in premature, female neonates, there are as of yet no
Marie Mitani-Konno, Marie Mitani-Konno, Reiko Saito, Hiroko Narumi-Wakayama, Yuki Sakai, Yuki Sakai, Shuichi Suzuki, Hiroyuki Satoh, Yukihiro Hasegawa, Yukihiro Hasegawa   +9 more
doaj   +1 more source

A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue

The Turkish Journal of Pediatrics, 2020
Background. Aromatase deficiency leading to virilization in mother and female fetuses during pregnancy is a rare disease. It is characterized by impaired estrogen production, increased gonadotropins, and ovarian cysts. Case.
Sezer Acar, Ece Böber, Mustafa Olguner, Erdener Özer, Ayhan Abacı, Bayram Özhan, Semra Gürsoy, Tufan Çankaya, Hüseyin Onay, Ahu Paketçi, İbrahim Mert Erbaş, Korcan Demir   +11 more
doaj   +1 more source

An unusual case of type a posterior cloaca associated with 46xx disorder of sexual differentiation with y duplication of urethra

Journal of Indian Association of Pediatric Surgeons, 2022
We report an infant reared as a girl who presented with ambiguous genitalia and urine coming per rectum. On examination, she had minimal clitoromegaly with labial fusion and Y urethral duplication.
Rahul K Gupta, Pooja Tiwari, Sandesh V Parelkar, Beejal V Sanghvi, Kedar P Mudkhedkar, Satej S Mhaskar, Rujuta S Shah   +6 more
doaj   +1 more source