Cover Image

46, XX testicular disorder of sex development: A case report

Saved in:

Bibliographic Details
Main Author:	Krishnachaitanya Mantravadi (Author)
Format:	Book
Published:	Wolters Kluwer Medknow Publications, 2022-01-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

46XX testicular disorder of sex development
by: Krishna Chaitanya Mantravadi, et al.
Published: (2021)

46XX testicular disorder of sex development
by: Aasim N Maldar, et al.
Published: (2022)

A Korean boy with 46,XX testicular disorder of sex development caused by duplication
by: Gyung Min Lee, et al.
Published: (2014)

A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report
by: Eda Mengen, et al.
Published: (2020)

Leydig Cell Tumor in a Patient with 46,XX Disorder of Sex Development (DSD), Ovotesticular: A Case Report and a Review of the Literature
by: Steffen Gretser, et al.
Published: (2021)

The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review
by: Jianlong Zhuang, et al.
Published: (2021)

Ovotesticular disorder of sex development in a 46 XY adolescent: a rare case report with review of the literature
by: Koui Bbs, et al.
Published: (2023)

46,XY ovotesticular disorders of sex development: A therapeutic challenge
by: Maria-Grazia Scarpa, et al.
Published: (2017)

Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype
by: Silvano Bertelloni, et al.
Published: (2021)

Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
by: Shaohua Sun, et al.
Published: (2019)

GATA-4 Variants in Two Unrelated Cases with 46, XY Disorder of Sex Development and Review of the Literature
by: Nurullah Çelik, et al.
Published: (2022)

46, XY disorder of sex development (DSD) complicated by a serous borderline tumor of the ovary: a case report and review of the literature
by: Jiangying Zhao, et al.
Published: (2020)

Prenatal Diagnosis of 45,X/46,XX Mosaicism with Presence of SRY Gene. A Case Report
by: Pedro Alí Díaz-Véliz Jiménez, et al.
Published: (2013)

Craniofacial morphology in males with 46,XX chromosomal constitution
by: Šćepan Ivana, et al.
Published: (2003)

An unusual case of type a posterior cloaca associated with 46xx disorder of sexual differentiation with y duplication of urethra
by: Rahul K Gupta, et al.
Published: (2022)

Gonadal Dysgenesis 46, XX Associated with Mayer-Rokitansky-Kuster-Hauser Syndrome: One Case Report
by: N. Bousfiha, et al.
Published: (2010)

A 46,XX karyotype in men with infertility: Two new cases and review of the literature
by: Elisavet Kouvidi, et al.
Published: (2022)

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
by: Şenay Savaş-Erdeve, et al.
Published: (2021)

Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review
by: Jiansheng Wei, et al.
Published: (2022)

Socio-medical burden of managing a Nigerian child with 46XY male disorder of sex differentiation: A Case Report
by: Oba-Daini OO, et al.
Published: (2019)

A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome
by: Sriharibabu Manne, et al.
Published: (2016)

Mosaic 46,XX,der(9)t(9;13)(p24;q12)/46,XX at amniocentesis can be a culture artefact and associated with a favorable fetal outcome
by: Chih-Ping Chen
Published: (2023)

Yolk Sac Tumor of the Ovary in Mosaic 46XX Turner Syndrome
by: Suryawan AZ, et al.
Published: (2024)

A 46,XX Male Adolescent Presenting with a Chief Complaint of Gynecomastia
by: Min Sun Kim, et al.
Published: (2015)

A Rare Case of 46, XX (SRY+) With Normal Male Stature and Unilateral Absence of the Vas Deferens
by: Ganbayar Batmunkh, et al.
Published: (2021)

46 xy ovotesticular disorder: A rare case report with review of literature
by: Bhati Meenal, et al.
Published: (2021)

Gender dysphoria in 46,XX persons with adrenogenital syndrome raise as females. A correction.
by: Ricardo eGonzález, et al.
Published: (2015)

Case Report: De novo variant in myelin regulatory factor in a Chinese child with 46,XY disorder/difference of sex development, cardiac and urogenital anomalies, and short stature
by: Hui Wang, et al.
Published: (2022)

A Rare Case of Rudimentary Uterus With Absence of Both Ovaries and 46,XX Normal Karyotype Without Mosaicism
by: Murat Dede, et al.
Published: (2008)

A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene
by: Eda Mengen, et al.
Published: (2020)

Identification of novel variants and candidate genes in women with 46,XX complete gonadal dysgenesis
by: Leilei Ding, et al.
Published: (2024)

Investigation of <it>KIT</it> gene mutations in women with 46,XX spontaneous premature ovarian failure
by: Nelson Lawrence M, et al.
Published: (2002)

The identification of a spontaneous 47, XX, +21/46, XY chimeric fetus with male genitalia
by: Lee Kuei-Fang, et al.
Published: (2012)

Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2022)

A novel c.64G > T (p.G22C) NR5A1 variant in a Chinese adolescent with 46,XY disorders of sex development: a case report
by: Dan Zhang, et al.
Published: (2023)

Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birth
by: Chih-Ping Chen
Published: (2024)

Prenatal diagnosis of holoprosencephaly associated with Smith-Lemli-Opitz syndrome (SLOS) in a 46,XX fetus
by: André Travessa, et al.
Published: (2017)

Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism
by: Malgorzata A. Krawczyk, et al.
Published: (2022)

Prenatal diagnosis and genetic counseling of 45,X/46,XX low-level mosaicism with a favorable outcome
by: Xia Gao, et al.
Published: (2024)

45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line
by: Chih-Ping Chen, et al.
Published: (2022)