Results 31 to 40 of about 167,426,214 (275)

Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin

open access: yesJCRPE, 2021
We describe a 46,XX girl with Denys-Drash syndrome, showing both kidney disease and genital abnormalities, in whom a misdiagnosis of hyperandrogenism was made.
Carla Bizzarri   +11 more
doaj   +1 more source

Uruguay Sustainable Development Report 2021 [PDF]

open access: yes, 2021
Este informe presenta una edición especial del índice de los ODS y los tableros de control para Uruguay. Uruguay se compara con los países de la OCDE utilizando un conjunto específico de indicadores de los ODS disponibles para estos países.
Inter-American Development Bank
core   +1 more source

Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2019
Purpose Patients with ovotesticular disorder of sex development (DSD) and mixed gonadal dysgenesis (MGD) usually present with asymmetric gonads and have wide phenotypic variations in internal and external genitalia.
Yoon Myung Kim   +4 more
doaj   +1 more source

Spreading the clinical window for diagnosing fetal-onset hypogonadism in boys

open access: yesFrontiers in Endocrinology, 2014
In early fetal development, the testis secretes –independently of pituitary gonadotropins– androgens and anti-Müllerian hormone (AMH) which are essential for male sex differentiation.
Rodolfo eRey
doaj   +1 more source

Barriers in access to healthcare services for individuals with disorders of sex differentiation in Bangladesh: an analysis of regional representative cross-sectional data

open access: yesBMC Public Health, 2020
Background Worldwide people in disorder of sex development (DSD) faces multiple barriers while seeking their social rights, particularly healthcare services. We aimed to explore the healthcare opportunities available to them, using patterns of healthcare
Alam Khan   +13 more
doaj   +1 more source

Progress Report (2014-2015) of the MDB Working Group on Sustainable Transport [PDF]

open access: yes, 2015
1. In the third year of the Multilateral Development Banks¿1 (MDBs) Joint Statement of 2012, our eight MDBs are on target to meet the goal of the Commitment to Sustainable Transport (hereafter the Rio+20 Commitment) to provide more than $175 billion of ...
Inter-American Development Bank
core   +1 more source

Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review

open access: yesBMC Medical Genomics, 2022
Background 46,XX male disorders of sex development are rare. Approximately 80% of cases of testicular tissue differentiation may be due to translocation of SRY to the X chromosome or an autosome. SRY-negative 46,XX males show overexpression of pro-testis
Jiansheng Wei   +5 more
doaj   +1 more source

Bilateral Cryptorchidism, a rare presentation for persistent Müllerian duct syndrome

open access: yesElectronic Physician, 2016
Persistent Müllerian duct syndrome (PMDS) is a rare, sex-limited, autosomal recessive disorder representing male pseudo-hermaphroditism. It is observed in males with the presence of female reproductive organs such as the uterus, cervix, and bilateral ...
Abdullah Al-Faris   +3 more
doaj   +1 more source

Male refractory hypospadias with sexual reversal: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Hypospadias is one of the most prevalent urogenital malformations in clinic. However, some hypospadias may have a more complex disorder of sex development. Usually, hypospadias in these patients is severe.
Jianfeng Zhao   +3 more
doaj   +1 more source

Pituitary Macroadenoma in a Girl with Male Karyotype: A Rare Case Study

open access: yesActa Medica Indonesiana, 2023
Macroadenoma is a tumor that typically develops in the epithelial cells of the pituitary gland. Patients suffering from the condition are often asymptomatic with complaints that are caused by hormonal imbalance. Therefore, chromosome analysis needs to be
Fatinah Shahab   +5 more
doaj   +2 more sources

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