hrp0095p1-261 | Diabetes and Insulin | ESPE2022

Parental stress in children with type 1 diabetes from different socioeconomic backgrounds

Levy-Khademi Floris , Heifetz Eliyahu , Avnon-Ziv Carmit , Auerbach Adi , Birnbaum Hanna

Background: Type 1 diabetes is one of the most common chronic diseases in childhood. Parents of children with type 1 diabetes are significantly involved in the treatment, rendering them vulnerable to parental stress. Psychological difficulties experienced by the parents may have adverse effects on disease management and the child's psychological and somatic health.Objectives: To assess parental stress and factors in...

hrp0097p1-37 | Diabetes and Insulin | ESPE2023

Dietary Intake in Children and youth with Type 1 Diabetes from Different Ethnic Backgrounds and its Relation to Different Metabolic Parameters

M. Heifetz Eliyahu , Avnon- Ziv Carmit , Auerbauch Adi , Dagan Tal , Hershkop Karen , Levy-Khademi Floris

Background: Medical nutrition therapy is one of the cornerstones of the treatment of type 1 diabetes. Nutrition is affected by many factors including ethnicity, socioeconomic background, and culture.Objectives: To evaluate the nutritional status in a cohort of children with type 1 diabetes from different ethnic backgrounds and to seek differences among the groups. In addition determine the effect of nutrition on metaboli...

hrp0094p1-184 | Pituitary B | ESPE2021

The pituitary gonadal axis is not responsive to GnRH administration in PCSK 1 dysfunction

Mendelsohn Espen Eliyahu , Lavi Eran , Cahn Ranit , Sharaf Muna , Abu Libdeh Abdulsalam , Zangen David ,

Introduction: Patients homozygous for mutation in the PCSK-1 gene present clinically with severe congenital diarrhea and variable hormonal defects due to lack of enzyme/prohormone processing by Prohormone Convertase 1/3 (PC1/3). Although absence of spontaneous puberty has been reported in patients with PCSK-1 mutations, no peptide hormone(s) in the hypothalamus-pituitary-gonadal axis (HPG) have been reported to be dependent on PC1/3 cleavage. Here we studied t...

hrp0095p1-373 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2022

A novel Androgen Receptor mutation causes complete androgen receptor insensitivity syndrome with gender dysphoria and unusual postnatal androgen profile.

Cohen Amitay , Florsheim Nathan , Levy-Lahad Efrat , Eliyahu Mendelsohn Espen , Lavi Eran , Kerem Liya , Abu Libdeh Abdulsalam , Zangen David

Background: Androgen Insensitivity syndrome (AIS), the most common cause of XY DSD, is an X-linked recessive allelic disorder caused by Androgen Receptor (AR) gene mutations. The complete form (CAIS) stems from abrogation of AR activity and is characterized by an external female phenotype and scarce pubic hair, as well as lack of Mullerian structures. Postnatal gonadotropin and testosterone levels are not increased, and the classical ‘Mini-puberty’...