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]
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
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
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
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
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
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]
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?
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
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
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

