Cargando…

Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review

Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora. In the present study, the frequency of testicular malignancy in prepu...

Descripción completa

Detalles Bibliográficos
Autores principales:	Barros, Beatriz Amstalden, de Oliveira, Letícia Ribeiro, Surur, Cíntia Regina Crocetti, Barros-Filho, Antonio de Azevedo, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society of Pediatric Endocrinology 2021
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026333/ https://www.ncbi.nlm.nih.gov/pubmed/33819955 http://dx.doi.org/10.6065/apem.2040170.085

Ejemplares similares

SUN-086 Pilot Study Using Aromatase Inhibitor in Puberty of Boys With Partial Androgen Insensitivity: Report of Three Cases
por: Maciel-Guerra, Andrea Trevas, et al.
Publicado: (2020)

Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
por: Cunha, Sarah Crestian, et al.
Publicado: (2018)

Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency
por: Veiga-Junior, Nélio Neves, et al.
Publicado: (2012)

Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males
por: Gabriel Ribeiro de Andrade, Juliana, et al.
Publicado: (2014)

Severe forms of partial androgen insensitivity syndrome due to p.L830F novel mutation in androgen receptor gene in a Brazilian family
por: Petroli, Reginaldo J, et al.
Publicado: (2011)

Complete androgen insensitivity syndrome with a large gonadal serous papillary cystadenofibroma
por: Ozdemir, Ozhan, et al.
Publicado: (2014)

Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants
por: dos Santos, Ana Paula, et al.
Publicado: (2013)

Androgens by immunoassay and mass spectrometry in children with 46,XY disorder of sex development
por: Oliveira, Letícia Ribeiro, et al.
Publicado: (2020)

Two cases of gonad retention in adolescent patients with complete androgen insensitivity syndrome (CAIS)
por: Nemivant, Samantha M., et al.
Publicado: (2019)

Leydig and Sertoli cell function in individuals with genital ambiguity, 46,XY karyotype, palpable gonads and normal testosterone secretion: a case-control study
por: Guaragna-Filho, Guilherme, et al.
Publicado: (2022)

Gonadal Tissue Cryopreservation for a Girl With Partial Androgen Insensitivity Syndrome
por: Finney, Esther L, et al.
Publicado: (2019)

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis
por: de Oliveira, Felipe Rodrigues, et al.
Publicado: (2023)

Bilateral Gonadal Cysts and Late Diagnosis of Androgen Insensitivity Syndrome Treated by Laparoscopic Gonadectomy
por: Tourlakis, D., et al.
Publicado: (2011)

OR05-1 Testicular Magnetic Resonance Imaging (MRI) Findings and Predictive Factors of Gonadal Neoplasia in Complete Androgen Insensitivity Syndrome
por: Carvalho, Filomena Marino, et al.
Publicado: (2022)

Complete Androgen Insensitivity Syndrome in Three Sisters
por: Verim, Levent
Publicado: (2014)

An Early Case of Complete Androgen Insensitivity Syndrome
por: Matalka, Leen, et al.
Publicado: (2023)

SAT-213 Late Diagnosis of Complete Androgen Insensitivity
por: Tsai, Karen, et al.
Publicado: (2019)

Complete Androgen Insensitivity Syndrome: From Bench to Bed
por: Tyutyusheva, Nina, et al.
Publicado: (2021)

Complete Androgen Insensitivity and Decreased Bone Mineral Density
por: Bauer, Elizabeth M, et al.
Publicado: (2021)

SUN-078 Clinical, Hormonal, Psychosexual Aspects, Gonadal Tumors and Genetic Background of an Androgen Insensitivity Syndrome Cohort
por: Batista, Rafael Loch, et al.
Publicado: (2020)

SUN-018 Epigenetic Loss of the PIWI/piRNA Machinery in Gonadal Tumors in Androgen Insensitivity Syndrome
por: Batista, Rafael, et al.
Publicado: (2019)

FSH may be a useful tool to allow early diagnosis of Turner syndrome
por: Carpini, Stela, et al.
Publicado: (2018)

A Novel Mutation of Androgen Receptor Gene in Complete Androgen Insensitivity Syndrome
por: Narumi, Satoshi, et al.
Publicado: (2007)

Role of Imaging in the Diagnosis and Management of Complete Androgen Insensitivity Syndrome in Adults
por: Nezzo, Marco, et al.
Publicado: (2013)

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene
por: Lucas-Herald, A., et al.
Publicado: (2016)

Comment on “Complete Androgen Insensitivity Syndrome: Optimizing Diagnosis and Management”
por: Balsamo, Antonio, et al.
Publicado: (2014)

Genetic analysis of a family with complete androgen insensitivity syndrome
por: Kota, Sunil Kumar, et al.
Publicado: (2013)

Laparoscopic gonedectomy in a case of complete androgen insensitivity syndrome
por: Bhaskararao, G., et al.
Publicado: (2014)

Potential risk of inguinal hernia in complete androgen insensitivity syndrome
por: Kimizuka, Yu, et al.
Publicado: (2022)

Induction of lactation in a patient with complete androgen insensitivity syndrome
por: Voon, Kimberly, et al.
Publicado: (2023)

A study of splicing mutations in disorders of sex development
por: de Calais, Flavia Leme, et al.
Publicado: (2017)

Androgen insensitivity syndrome: a review
por: Batista, Rafael Loch, et al.
Publicado: (2018)

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome
por: WANG, SONG, et al.
Publicado: (2016)

Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism
por: Konrade, Ilze, et al.
Publicado: (2019)

A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication
por: Francese-Santos, Ana Paula, et al.
Publicado: (2022)

Response to: Comment on “Complete Androgen Insensitivity Syndrome: Optimizing Diagnosis and Management”
por: Laganà, Antonio Simone, et al.
Publicado: (2014)

Complete Androgen Insensitivity Syndrome: A Problem-Based Learning Case
por: Neff, Adam, et al.
Publicado: (2016)

Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy
por: Heo, You Jung, et al.
Publicado: (2018)

Different Clinical Presentations and Management in Complete Androgen Insensitivity Syndrome (CAIS)
por: Lanciotti, Lucia, et al.
Publicado: (2019)

Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
por: Singh, Pratibha, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_ueb68f3bvi2fl6ir51139u17qa