Results 31 to 40 of about 56,903 (162)

UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development [PDF]

open access: yes, 2011
It is paramount that any child or adolescent with a suspected disorder of sex development (DSD) is assessed by an experienced clinician with adequate knowledge about the range of conditions associated with DSD.
Wallace, A. Michael   +79 more
core   +1 more source

408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing

open access: yesInternational Journal of Endocrinology, 2016
Objective. To evaluate diagnosis, age of referral, karyotype, and sex of rearing of cases with disorders of sex development (DSD) with ambiguous genitalia. Methods. Retrospective study during 23 years at outpatient clinic of a referral center.
Georgette Beatriz De Paula   +21 more
doaj   +1 more source

Disorders of sex development: a study of 194 cases

open access: yesEndocrine Connections, 2018
Objective: To study the clinical profile and the management of patients with disorders of sex development (DSD). Design and setting: Retrospective study from a tertiary care hospital of North India.
R Walia   +4 more
doaj   +1 more source

Disorders of sex development: A 10 years experience with 73 cases from the Kashmir Valley

open access: yesIndian Journal of Endocrinology and Metabolism, 2019
Purpose: To present the clinical data, investigative profile, and management of patients with disorders of sex development (DSD) from the endocrine unit of a tertiary care university hospital.
Raiz Ahmad Misgar   +6 more
doaj   +1 more source

Prevalence of gene mutations in a Chinese 46,XY disorders of sex development cohort detected by targeted next-generation sequencing

open access: yesAsian Journal of Andrology, 2021
46,XY disorders of sex development (DSD) is characterized by incomplete masculinization genitalia, with gonadal dysplasia and with/without the presence of Müllerian structures. At least 30 genes related to 46,XY DSD have been found. However, the clinical
Bing-Qing Yu   +6 more
doaj   +1 more source

46, XY disorder of sex development (DSD) complicated by a serous borderline tumor of the ovary: a case report and review of the literature

open access: yesDiagnostic Pathology, 2020
Background Patients with 46, XY disorder of sex development (DSD) are predisposed to the development of gonadal tumors, particularly germ cell tumors and gonadoblastoma.
Jiangying Zhao   +4 more
doaj   +1 more source

The use of genetics for reaching a diagnosis in XY DSD [PDF]

open access: yes, 2022
Reaching a firm diagnosis is vital for the long-term management of a patient with a difference or disorder of sex development (DSD). This is especially the case in XY DSD where the diagnostic yield is particularly low.
Alimusina, Malika   +7 more
core   +1 more source

DHX37 and 46, XY DSD : A new Ribosomopathy?

open access: yes, 2022
International audienceRecently, a series of recurrent missense variants in the RNA-helicase DHX37 have been reported associated with either 46,XY gonadal dysgenesis, 46,XY testicular regression syndrome (TRS), or anorchia.
Pailhoux, Eric   +2 more
core   +1 more source

Frequency of associated features in 46,XY and 46,XX Differences of sexual development (DSD) patients

open access: yes, 2022
Context: The focus of care in differences of sexual development (DSD) is mainly directed towards sex and gender development. Associated features are scarcely described. Widening the phenotypic spectrum of DSD might help to elucidate molecular aetiologies.
LUPI, V.
core   +1 more source

Cytogenetic and molecular insight into the genetic background of disorders of sex development in seventeen cats

open access: yesScientific Reports, 2022
The genetic background of feline disorders of sex development (DSDs) is poorly understood. We performed comprehensive cytogenetic, molecular, and histological studies of 17 cats with abnormal external genitalia, unusual behavior, or tricolor coats ...
Monika Stachowiak   +12 more
doaj   +1 more source

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