Results 101 to 110 of about 3,098 (225)

High prevalence of polycystic ovary syndrome in women with mild hirsutism and no other significant clinical symptoms [PDF]

, 2009
OBJECTIVE: To verify the conclusions of the Endocrine Society Guidelines that patients with mild hirsutism and no other important clinical signs (menstrual irregularities, infertility, central obesity, acanthosis nigricans, rapid progression of the ...
CARMINA, Enrico, DI FEDE, Gaetana, MANSUETO, Pasquale, PEPE, Ilenia, RINI, Giovam Battista   +4 more
core  

Odevixibat as an adjunctive treatment for refractory pruritus in rare variants of cholestatic liver disease

JPGN Reports, Volume 5, Issue 3, Page 296-302, August 2024.
Abstract Objectives Odevixibat, a reversible ileal bile acid transport inhibitor, has been shown to reduce serum bile acids (sBA) and pruritus mostly in children with progressive familial intrahepatic cholestasis (PFIC) 1 and 2 in clinical trials and case reports.
Akshat Goel, Bethany Tucker, Lorena Soler Casale, Tassos Grammatikopoulos   +3 more
wiley   +1 more source

Clitoral choristoma: A rare case report

Journal of Indian Association of Pediatric Surgeons, 2017
Clitoral hypertrophy is usually seen as a congenital malformation, specifically during the stages of hormonal expressions in the disorders of sexual development. Acquired clitoral hypertrophy is a relatively rare condition.
Jayalaxmi Shripati Aihole, Hemalatha Lokanath, M Narendra Babu, J Deepak   +3 more
doaj   +1 more source

Ovarian stromal tumor with minor sex-cord element with virilizing menifestations: a rare case report [PDF]

, 2017
Sex cord stromal tumor is a rare variety of ovarian tumor. These tumor have association with testosterone production which lead to virilisation in females.
Chaudhary, Usha Kumari, Kumar, Arvind, Mahajan, Neelam, Sharma, Ajay, Sharma, Reena, Vij, Anju   +5 more
core   +2 more sources

Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures

Clinical Genetics, Volume 105, Issue 6, Page 596-610, June 2024.
Expanding the phenotypic and molecular spectrum in lethal arthrogryposis. Abstract Multiple congenital contractures (MCC) due to fetal akinesia manifest across a broad spectrum of diseases, ranging from mild distal arthrogryposis to lethal fetal akinesia deformation sequence.
Gozde Tutku Turgut, Umut Altunoglu, Cagri Gulec, Tugba Sarac Sivrikoz, Tuğba Kalaycı, Guven Toksoy, Şahin Avcı, Behiye Tuğçe Yıldırım, Gözde Yeşil Sayın, Ibrahim Halil Kalelioglu, Birsen Karaman, Recep Has, Seher Başaran, Atil Yuksel, Hülya Kayserili, Zehra Oya Uyguner   +15 more
wiley   +1 more source

A case study in unethical transgressive bioethics: Letter of concern from bioethicists about the prenatal administration of dexamethasone. [PDF]

, 2010
On February 3, 2010, a Letter of Concern from Bioethicists, organized by fetaldex.org, was sent to report suspected violations of the ethics of human subjects research in the off-label use of dexamethasone during pregnancy by Dr. Maria New.
Brent, Robert L, Chervenak, Frank A, Hippen, Benjamin, McCullough, Laurence B   +3 more
core   +1 more source

Prenatal diagnosis and in utero treatment of congenital adrenal hyperplasia: An up‐to‐date comprehensive review

Prenatal Diagnosis, Volume 44, Issue 5, Page 635-643, May 2024.
Abstract Congenital adrenal hyperplasia (CAH) is a term that encompasses a wide range of conditions that affect the adrenals. Diagnosis and treatment before birth are important as irreparable birth defects can be avoided, decreasing the need for surgical intervention later in life, especially regarding genitalia anomalies. Although early implementation
Oluwateniayo O. Okpaise, Hyunyoung Ahn, Gabriele Tonni, Rodrigo Ruano   +3 more
wiley   +1 more source

Androgen deficiency in women [PDF]

, 2010
As evidências sugerem que a deficiência androgênica na mulher exibe como principal manifestação clínica a disfunção sexual, especialmente a queda da libido.
ALDRIGHI, José Mendes, AOKI, Tsutomu, FONSECA, Helena Proni, SCAPINELLI, Alessandro   +3 more
core   +2 more sources

Imaging features, clinical characteristics and neonatal outcomes of pregnancy luteoma: A case series and literature review

Acta Obstetricia et Gynecologica Scandinavica, Volume 103, Issue 4, Page 740-750, April 2024.
Distinguishing pregnancy luteoma from malignant ovarian tumors may be challenging. However, features such as maternal masculinization and the presence of solid masses with multiple nodules on imaging may provide valuable diagnostic clues. Abstract Introduction This study aimed to investigate the imaging features, clinical characteristics and neonatal ...
Jian‐Hong Shang, Cai‐Xin Huang, Qiao Zheng, Jie‐Ling Feng, Ke He, Hong‐Ning Xie   +5 more
wiley   +1 more source

Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia. [PDF]

, 2015
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 ...
Hayat, Marium, Rizwan, Azra
core   +1 more source