hrp0092p1-237 | Multisystem Endocrine Disorders | ESPE2019

The Effects of Fetal Electromagnetic Field Exposure on Expression of Anxiety Behavior and Associated Genes in Adolescent Period

OKSUZ Hale , OCAL Isil , AKILLIOGLU Kubra , ILGAZ Nermin Seda , OZPAK Lutfiye , KARACAY Seray , OKSUZ Halil Ibrahim , COBAN Fatma , SANGUN Levent , YILMAZ Mehmet Bertan

The stimulants that the mother is exposed during pregnancy may affect the baby in the future. Electromagnetic field exposure is an important external stimulus that we are subject to. In addition to the interaction of the earth and the sun with the magnetic field of man; nowadays the intensive use of electrical appliances, computers, mobile phones and internet, how electromagnetic field exposure may affect future generations will only occur in the continuation of our generation...

hrp0092p3-216 | Pituitary, Neuroendocrinology and Puberty | ESPE2019

Family Central Early Puberty about Three Sisters

safi wajdi , Hadj Kacem Faten , Ben Mrad Fatma , El Arbi Kawthar , Gargouri Imene , Rekik nabila , Charfi Nadia , Mnif Feki Mouna , Abid Mohamed

Introduction: Early puberty is defined in the girl by the appearance of secondary sexual characteristics before the age of 8 years. Unlike the boy, the central origin is most often idiopathic. The familial nature encourages looking for a genetic mutation which can explain this early maturation of the gonadotropic axis.Cases: These are three girls from a consanguineous marriage. They had no particular pathological anteced...

hrp0092p3-221 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2019

Gonadal Dysgenesis, 46 XY About 5 Familial Cases

Safi Wajdi , Hadj Kacem Faten , Ben Mrad Fatma , Gargouri Imene , Belabed Wafa , Rekik Nabila , Charfi Nadia , Rhouma Bochra Ben , Mnif Feki Mouna , Belghith Neila , Abid Mohamed

Introduction: Sexual disorders 46 XY are responsible for a range of phenotypic disorders; from an ambiguous phenotype to a complete female phenotype. This is often a sporadic condition. In this context, we report 5 cases of gonadal dysgenesis, 46 XY belonging to the same family and particular phenotypic expression. this particular phenotype arise a question about the link between familial sexual differenciation disorders and the panel of genes involved in sexu...

hrp0082p1-d3-13 | Adrenals & HP Axis (1) | ESPE2014

Assessment of Blood Pressure and Left Ventricular Parameters in Children with Classical CAH-due to 21 Hydroxylase Deficiency

Abdelghaffar Shereen , Ibrahim Reem , Abdelaziz Osama , Hafez Mona , Mamdouh Mona , Alashmawy Abeer , Elmougy Fatma , Abdelaty Sahar , Ibrahim Amany , Mehawed Hend , Ghaly Isis

Background: Patients with congenital adrenal hyperplasia (CAH), due to 21 hydroxylase (OH) deficiency may develop an adverse cardiovascular risk profile as reported by few previous studies.Objective and Hypotheses: Blood pressure (BP) and echo parameters in children with CAH due to 21-OH deficiency were evaluated.Method: This cross-sectional study included 53 children. BP, echocardiographic left ventricular functions as well as gro...

hrp0084p2-410 | GH & IGF | ESPE2015

Response to GH Treatment in the Very Young with GH Deficiency

Cetinkaya Semra , Poyrazoglu Sukran , Aycan Zehra , Siklar Zeynep , Berberoglu Merih , Atay Zeynep , Bereket Abdullah , Ercan Oya , Mengen Eda , Demirel Fatma , Darcan Sukran , Darendeliler Feyza

Aim: Data on response to GH treatment in the very young children with GH deficiency is scarce. The aim of this study was to evaluate the growth response in such children in a national multicentre study and to analyse the factors affecting the growth response.Materials and methods: In this study, we retrospectively evaluated the files of GH deficiency patients who had started GH treatment between 0–3 years of age who were being followed in 14 differe...

hrp0084p3-582 | Adrenals | ESPE2015

Rapid Molecular Diagnosis of CAH by Strip Hybridisation Assay in DEMPU

El-Mougy Fatma , Hafez Mona , Atty Sahar Abdel , Ibrahim Amany , Mehawed Hend , Musa Noha , Ekladious Sherif , Elsharkawy Marwa , Abdullatif Mona , Afif Alaa , Baz Heba El

Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder in which more than 90% of CAH cases are caused by mutations of the 21-hydroxylase (CYP21A2) gene.Objective and hypotheses: To determine the mutational spectrum in Egyptian CAH patients attending Diabetes Endocrine and Metabolism Pediatric Unit (DEMPU) including family members of CAH patients.Method: The use of reverse hybridization assay for the mol...

hrp0097fc5.2 | Diabetes and insulin 1 | ESPE2023

Nailfold capillaroscopy: An alternative non-invasive tool for evaluating microvascular involvement in children with type 1 diabetes

Cakmak Figen , İnan Balci Elif , Yildiz Melek , Gul Demirkan Fatma , Yetim Sahin Aylin , Poyrazoglu Sukran , Bas Firdevs , Darendeliler Feyza , Aktay Ayaz Nuray

Background: Type 1 diabetes (T1D) is characterized by chronic hyperglycemia and microvascular complications like retinopathy, nephropathy, and neuropathy in long term. Nailfold video capillaroscopy (NVC) is a non-invasive method used to examine the microcirculation in the skin. In this study, we aimed to evaluate the microvascular structure in T1D with NVC, observe capillaroscopic alterations, and reveal the relationship of capillaroscopic abnormalities with g...

hrp0098p2-290 | Thyroid | ESPE2024

Graves disease in children and adolescents, results of a multicenter Algerian study

Bensalah Meryem , Boulesnanae Kamelia , Bouferoua Fadila , Bessahraoui Mimouna , Djermane Adel , Kherra Sakina , Selim Nihad , Abes Hakima , Iabbassen Malek , Berkoune Fatma , Taazibt Akli , Chanegriha Mounira , Laadjouz Asmahane , Ouarezki Yasmine

Background: Graves’ disease (GD) is a rare autoimmune affection in children with a female predominance. Its prevalence is about 0,1/100 000py in children and 3/100 000 py in adolescents and characterized by more important frequency of relapse than adults after medical treatment.Aim: Is to evaluate clinical biological radiological and treatment outcome of children and adolescents affected by GD in nine Algerian hosp...

hrp0098p3-292 | Late Breaking | ESPE2024

Is the diary for self-monitoring of blood glucose levels in children with diabetes reliable?

Salih Bendeddouche Ahmed , Boukli-Hacene Chakib , Benasla Djihane , Senouci Djawida , Mazari Wafa , Wahiba Hamidi Fatma , Benchikh Sana , Bouriche Khadidja , Belbachir H.L

Objective: To evaluate the reliability and accuracy of diary entries in relation to glucometer memory in children with T1D and its impact on mid-term glycemic outcomes.Material and method: The SMBG (Self-monitoring blood glucose) in the diaries were compared to the readings from the memory of the glucometer conforming to the international standard ISO 15197 by the ''EMPECS'' software in 2 groups of 10...

hrp0098p3-293 | Late Breaking | ESPE2024

Impact of Ramadan fasting on young people with diabetes type 1

Salih Bendeddouche Ahmed , Boukli-Hacene Chakib , Benasla Djihane , Benchikh Sana , Senouci Djawida , Wahiba Hamidi Fatma , Mazari Wafa , Bouriche Khadidja , Belbachir H.L

Introduction: Fasting is observed throughout the day when daylight is visible, or as mentioned in the Qur'an: "Eat and drink until the white thread of dawn becomes distinct to you from the black thread of night. Although patients with type 1 diabetes are medically exempt from this obligation, many insist on fasting during Ramadan. To date, healthcare providers have given conflicting advice on the feasibility of fasting during the month of Ramadan.</p...