Results 111 to 120 of about 30,274 (252)

Embryonal carcinoma in androgen insensitivity syndrome

Indian Journal of Medical and Paediatric Oncology, 2011
AbstractEmbryonal cell carcinoma is a rare clinical entity. We report a case of a 20-year-old patient who presented with lump lower abdomen for last two months with primary amenorrhea and poorly developed secondary sexual characteristics. Ultrasonography (USG) whole abdomen showed lower abdominal mass approximately 15΄15΄10 cm, probably neoplastic ...
Rahman Hafizur, Amal Chandra Kataki, Debabrata Barmon, Jagannath Dev Sharma   +3 more
openaire   +2 more sources

Novel Mutations Segregating with Complete Androgen Insensitivity Syndrome and Their Molecular Characteristics

International Journal of Molecular Sciences, 2019
We analyzed three cases of Complete Androgen Insensitivity Syndrome (CAIS) and report three hitherto undisclosed causes of the disease. RNA-Seq, Real-timePCR, Western immunoblotting, and immunohistochemistry were performed with the aim of characterizing ...
A. Malcher, P. Jędrzejczak, T. Stokowy, Soroosh Monem, K. Nowicka-Bauer, A. Zimna, A. Czyżyk, M. Maciejewska-Jeske, B. Męczekalski, K. Bednarek-Rajewska, A. Wozniak, N. Rozwadowska, M. Kurpisz   +12 more
semanticscholar   +1 more source

The Physiological, Psychological and Genetic Expressions of XY Female Reporting at Tertiary Care Infertility Clinic of Kingdom of Saudi Arabia

Pakistan Journal of Medical Research, 2022
Background: Disorder in sex development (DSD) refers to a variety of diagnoses in which the development of chromosomal make-up, gonadal development, or anatomical development is abnormal.
Munazzah Rafique, Dania Al Jaroudi
doaj   +2 more sources

Complete Androgen Insensitivity Syndrome: A Problem-Based Learning Case

MedEdPORTAL, 2016
Introduction To address the lack of medical education on lesbian, gay, bisexual, transgender, queer (LGBTQ), and difference in sex development–affected (DSD-affected) individuals, the University of Louisville initiated the eQuality project.
Adam Neff, Suzanne Kingery
doaj   +1 more source

Is A Quantum Stabilizer Code Degenerate or Nondegenerate for Pauli Channel? [PDF]

arXiv, 2010
Mapping an error syndrome to the error operator is the core of quantum decoding network and is also the key step of recovery. The definitions of the bit-flip error syndrome matrix and the phase-flip error syndrome matrix were presented, and then the error syndromes of quantum errors were expressed in terms of the columns of the bit-flip error syndrome ...
arxiv  

Two cases of gonad retention in adolescent patients with complete androgen insensitivity syndrome (CAIS)

Journal of Pediatric Surgery Case Reports, 2020
Bilateral gonadectomy was the historical recommendation for patients diagnosed with complete androgen insensitivity syndrome (CAIS) due to the perceived risk of malignancy in the gonads.
Samantha M. Nemivant, Kathleen van Leeuwen, Erica M. Weidler   +2 more
doaj  

Syndrome Measurement Order for the [[7,1,3]] Quantum Error Correction Code [PDF]

arXiv, 2013
In this work we explore the accuracy of quantum error correction depending of the order of the implemented syndrome measurements. CSS codes require bit-flip and phase flip-syndromes be measured separately. To comply with fault tolerant demands and to maximize accuracy this set of syndrome measurements should be repeated allowing for flexibility in the ...
arxiv  

Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II)

Journal of Clinical Endocrinology and Metabolism, 2018
Context Inactivating mutations within the AR gene are present in only ~40% of individuals with clinically and hormonally diagnosed androgen insensitivity syndrome (AIS).
N. Hornig, Pascal Rodens, H. Dörr, N. Hubner, A. Kulle, H. Schweikert, M. Welzel, S. Bens, O. Hiort, R. Werner, Susanne Gonzalves, A. Eckstein, M. Cools, Annemarie Verrijn-Stuart, H. Stunnenberg, R. Siebert, O. Ammerpohl, P. Holterhus   +17 more
semanticscholar   +1 more source

Partial androgen insensitivity syndrome presenting as pubertal gynecomastia: clinical and hormonal findings and a novel mutation in the androgen receptor gene

Endocrinology, Diabetes & Metabolism Case Reports, 2018
Pubertal gynecomastia is common, can be seen in 65% of the adolescent boys and is considered physiological. It is thought to be due to transient imbalance between the ratio of testosterone and estradiol in the early stages of puberty.
Priya Vaidyanathan, Paul Kaplowitz
doaj   +1 more source

Carrier detection in the testicular feminisation syndrome: deficient 5 alpha-dihydrotestosterone binding in cultured skin fibroblasts from the mothers of patients with complete androgen insensitivity. [PDF]

, 1984
Malcolm B. Hodgins, E M Duke, D Ring
openalex   +1 more source