hrp0098con1 | Should we restrict height in tall stature? | ESPE2024

Controversy: Should we restrict height in tall stature?

Sävendahl Lars Sävendahl , Witchel Selma

Following exclusion of specific medical disorders such as gigantism, tall stature is generally not considered a severe somatic problem. Orthopedic concerns such as scoliosis and kyphosis may occur. In addition, higher incidences of psychological strug gles, such as social anxiety, social withdrawal and less assertiveness, have been observed. Tall stature is associated with practical difficulties such as finding appropriate bedding, shoes and clothing. Activities of daily livin...

hrp0092p1-142 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2019

Disorders of Sex Development (DSD): Inconsistencies Between Clinical Features and Peripheral Blood Cultured Karyotypes

Gurtunca Nursen , Yatsenko Svetlana , Schneck Francis , Witchel Selma Feldman

Sex differentiation and development are complex processes reflecting the precise spatiotemporal expression of specific genes and interactions among gene products. In some instances, peripheral blood karyotype diverges from anticipated findings based on phenotypic features. Ascertaining for chromosomal mosaicism aids the shared decision-making discussions with families and other health care providers. We have investigated for sex chromosome mosaicism in 13 patients by using flu...

hrp0094p2-409 | Sex differentiation, gonads and gynaecology or sex endocrinology | ESPE2021

Surprising X Chromosomes: Unusual Mosaicism

Zorkot Zeinab , Yatsenko Svetlana , Garibaldi Luigi , Witchel Selma

Background: Among 46,XY individuals, androgen insensitivity syndrome (AIS) due to deleterious variants of the androgen receptor (AR) gene is one cause for a difference of sexual development (DSD). Typically, individuals with complete androgen insensitivity syndrome (CAIS) present with female external genitalia and palpable labial masses. Whereas most patients carry germline variants inherited in an X-linked manner, approximately 30% of patients manifest de novo variants. We de...

hrp0097rfc7.2 | Sex differentiation, gonads and gynaecology or sex endocrinology | ESPE2023

International Evidence-Based Guidelines for PCOS 2023: Recommendations in Adolescent Girls

Witchel Selma , Pena Alexia , Hoeger Kathy , Oberfield Sharon , Teede Helena

Objective: The original consensus-based Rotterdam criteria, now evidence-based criteria, is recommended for the diagnosis of PCOS in adult women. These criteria state that PCOS can be diagnosed when two of three major criteria (anovulatory cycles, clinical/biochemical hyperandrogenism, and polycystic ovary morphology or elevated AMH levels) are present and other potential etiologies have been excluded. Use of these criteria in adolescent girls is problematic b...

hrp0089rfc8.3 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2018

Pharmacological Treatment of Adolescent Polycystic Ovary Syndrome (PCOS) According to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS

Pena Alexia , Witchel Selma , Hoeger Kathy , Oberfield Sharon , Vogiatzi Maria , Misso Marie , Teede Helena

The treatment of Polycystic Ovary Syndrome (PCOS) during adolescence is controversial. The aim of the international evidence-based guideline was to promote accurate diagnosis, optimal consistent care, prevention of complications and to improve patient experience and health outcomes. Extensive international health professional and patient engagement informed the priorities and core outcomes for the guideline. Internationally nominated panels including women with PCOS and a mult...

hrp0086fc7.4 | Gonads & DSD | ESPE2016

Disruption of Long-Range Transcriptional Regulation of Genes Known to be Associated with DSD

Yatsenko Svetlana , Madan-Khetarpal Suneeta , Schneck Francis , Hughan Kara , Rajkovic Aleksander , Witchel Selma

Background: Early genetic diagnosis in patients with disorders of sex development (DSDs) can facilitate clinical management, predict recurrence risks, and augment general knowledge. Novel techniques such as SNP microarrays, GWAS, and exome sequencing have identified mutations in the coding regions of genes linked to DSDs. In some instances, variants in non-coding regions have been associated with 46,XY gonadal dysgenesis, e.g. deletions upstream of SOX9 (PLoS One 2011...