hrp0098p3-6 | Adrenals and HPA Axis | ESPE2024

Induced Adrenal Insufficiency: Case series

Djermane Adel , Ouarezki Yasmina , Attal Asma , Maouche Hachemi

Background: Adrenal insufficiency (AI) is mainly due to congenital disorders in children. Acquired causes can be autoimmune, inflammatory, infectious but mainly drug induced especially due to prolonged exposure to excess glucocorticoids. Daily dose, duration, timing, as well as the route of administration can all play a role in. We present two patients with different clinical presentations.Case 1: A 8 year- old-girl refe...

hrp0097p1-593 | Thyroid | ESPE2023

Congenital malformations in permanent and transient congenital hypothyroidism – prevalence and etiology

Ouarezki Yasmina , Shepherd Sheila , Jones Jeremy , Abubaker Alghanay A , Smith Sarah , Shaikh Guftar , Donaldson Malcolm

Background: An increased prevalence of extra-thyroidal congenital malformations in infants with congenital hypothyroidism (CH) is well established. However, accurate estimation of prevalence figures requires careful distinction between permanent and transient CH. Moreover, the mechanisms resulting in congenital malformations are not well understood.Study aim: To estimate the prevalence of cardiac, extra-cardiac and/or sy...

hrp0098rfc7.4 | GH and IGFs | ESPE2024

Use of iSYS-IDS IGF1-Assay Normative Data as a STANDARD in the Diagnosis of Pediatric Growth Hormone Deficiency

Djermane Adel , Ouarezki Yasmina , Ladjouze Asmahane , Kherra Sakina , Mohammedi Kahina , Bensalah Meriem , Aitabdelkader Belaid , Maouche Hachemi

Background: Analysis of insulin-like growth factor-I (IGF-I) is an important tool in the diagnosis of growth hormone deficiency. However, there are significant differences between IGF-I assays and normative data sets, which may have important clinical implications. The aim of this study was to investigate the difference in Z-scores between the iSYS-IDS reference values and the reference values for the IGF-I specific assay used in children.<p class="abstext...

hrp0098p3-53 | Diabetes and Insulin | ESPE2024

Diabetic Neuropathic Cachexia and Mauriac Syndrome: A Rare Complication of Poorly Controlled Diabetes Mellitus

Djermane Adel , Fafa Abdennader , Ouarezki Yasmina , Ghedjati Asma , Kermi Lynda , Atek Laziz , Arous Radjaa , Semar Yasmine , Aggoune Samira , Maouche Hachemi

Background: Diabetic neuropathic cachexia is a rare syndrome of acute neuropathic pain and profound weight loss. Mauriac syndrome has rarely been reported in children and adolescents with a poorly controlled diabetes mellitus type 1. Common presenting features include short stature, growth retardation, moon facies, protuberant abdomen, and proximal muscle wasting. We report the first case of the association of Mauriac Syndrome and Diabetic neuropathic cachexia...

hrp0098p2-266 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2024

Outcome of antenatal treatment in congenital adrenal hyperplasia due to 21 hydroxylase-deficiency in Algeria

Ouarezki Yasmina , Cherfi Nadia , Abbas Wassila , Mimouni Leila , Djermane Adel , Mohammedi Kahina , Tardy Veronique , Menassa Rita , Roucher Florence , Ibsaine Ouardia , Bouzerar Zahir , Maouche Hachemi , Zeggane Houria , Ladjouze Asmahane

Introduction: 21-hydroxylase deficiency (21-OHD) is the most common cause of female virilisation at birth and carries heavy psychosocial consequences. Early antenatal treatment with dexamethasone is successful in avoiding severe virilisation, thus reducing the need for surgery and improving psychological outcome.Objectives: To evaluate the feasibility and effectiveness of antenatal treatment in 21-OHD in a resource-limit...