hrp0092p3-86 | Diabetes and Insulin | ESPE2019

Clinical Profile of Paediatric Patients with type 1 Diabetes Mellitus at a Tertiary Health Care Center in the Oriental Region of Northeastern Morocco

Ben Yakhlef Salma , Derkaoui Nada , Rouf Siham , Ezzerrouqi Amine , Latrech Hanane

Introduction: The growing pandemic of type 1 diabetes is considered as an enormous multifactorial public health challenge in the world. Many targeted interventions should be provided to improve type 1 diabetes management especially during childhood and adolescence.The purpose of this study is to elucidate the epidemiological, clinical and management profile of type 1 diabetes in Moroccan children and adolescents followed up in t...

hrp0094p2-491 | Thyroid | ESPE2021

Pediatric Graves’ disease in southern Tunisia

Kmiha Sana , Zghal Mohammed Ali , Chabchoub Imen , Ameur Salma Ben , Aloulou Hajer , Kammoun Thouraya

Background: Hyperthyroidism is uncommon in children. Graves’ disease is the most common cause in pediatric population. The diagnosis is based on the presence of anti-TSH receptor antibodies. Pediatric Graves’ disease has some peculiarities mainly in term of treatment and evolution, since its prognostic is different than adults.Aim: The aim of this study is to describe the epidemiological, clinical and biological features of pediatric Graves...

hrp0097p1-393 | Thyroid | ESPE2023

Primary hydatid cyst of the thyroid gland in a Libyan child

Ghawil Millad , Ben Omar Nesrin , Shatani Amal , Belhaj Salma , Doggah Milad

Background: Cervico-facial hydatid cyst is rare. It has a high incidence rate in regions with a mild climate such as Mediterranean countries, Middle East, South America, New Zealand, Australia and Southeast Asia. Hydatid cyst develops most often in the liver and lungs in human beings. The incidence of hydatid cysts in the thyroid gland is rare and it accounts for 1% of echinococcosis locations. Primary hydatid cyst of thyroid gland is an exceptional localizati...

hrp0097p2-229 | Thyroid | ESPE2023

What is the risk on intelligence in children with dysthyroiidism ?

Marzouk Asma , Braeik Amina , Ben Hssine Nahed , Laajili Mariem , Kefi Ahlem , Thebti rahma , Mzoughi oumaima , Ben Hssine Sarra , Friha farida , Bouaziz Asma

Introduction:Thyroid hormones are essential for early neurocognitive development as well as growth and development throughout childhood. The intelligence of children with dysthyroidism has been little evaluated.Objective:Assessing of the intelligence in children with dysthyroidism.Patients and methods: Descriptive prospective study carried out by applying the IQ in 26 patients aged...

hrp0097p2-167 | Thyroid | ESPE2023

Subclinical hypothyroidism in children: epidemiological study of 30 patients

Marzouk Asma , Ammar Mariem , Braik Amina , Laajili Mariem , Kefi Ahlem , thebti rahma , Mzoughi Oumaima , Friha farida , Ben Hssine Sarra , Bouaziz Asma

Introduction:Subclinical hypothyroidism (SH) is defined in children by a moderate rise in TSH (TSH: 4.5-10 mU/l) compared to a normal level of free T4. However, the clinical consequences remain a subject of controversy, hence the need to take a position on the relevance of treating it.Objective: Description of the clinical, biological and evolutionary characteristics of SH in children.Patie...

hrp0086p1-p690 | Endocrinology and Multisystemic Diseases P1 | ESPE2016

Fludrocortisone: A Treatment for Tubulopathy Post Paediatric Renal Transplantation – A Scottish Study

Rashid Salma , Athavale Deepa , Shaikh M Guftar

Background: Post renal transplantation, tubulopathies may occur as an effect of transplantation itself or secondary to the use of immunosuppressive regimes. This often requires administration of large doses of sodium bicarbonate and sodium chloride, resulting in poor compliance. Adult studies have shown the advantages of fludrocortisone in the treatment of severe tubulopathies post renal transplant. There is limited data in children. We report our experience from a tertiary pa...

hrp0092p3-240 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2019

Testicular Regression Syndrome A Clinical and Pathologic Study of 4 Cases

Khlifi Asmaa , Derkaoui Nada , Benyakhlef Salma , Yaden Youssef , Latrech Hanane

Introduction: Testicular regression syndrome (TRS) also called vanishing testes syndrome is a rare developmental disorder that represents less than 5% of cryptorchidism cases. It is characterized by the absence of one or both testicles with partial or complete absence of testicular tissue. TRS phenotypes are various depending on the extent and timing of the intrauterine accident during fetal sexual development.Material and Me...

hrp0094p2-168 | Diabetes and insulin | ESPE2021

Newly-onset type 1 diabetes mellitus triggered by COVID-19: Original case report

Benyakhlef Salma , Abdellaoui Wahiba , Derkaoui Nada , Rouf Siham , Latrech Hanane ,

Introduction: During this year, scientific research revolves around COVID-19, with so many unanswered queries in term of pathogenesis; complications, and mortality rate; in light of limited pediatric evidence. The close relation between COVID 19 and new-onset diabetes especially in children is still an unresolved issue. Our paper, exhibits an unique presentation of DKA misleading COVID 19 diagnosis at this ageCase presentation: A three-y...

hrp0097p1-221 | Bone, Growth Plate and Mineral Metabolism | ESPE2023

Celiac disease in a patient with Sclerosteosis: an association or just a co-incidence?

Abdelmeguid Yasmine , Riad Salma , Mokhtar Nada , Taha El-Hendawy Mahmoud

Sclerosteosis is a rare autosomal recessive disorder characterized by progressive skeletal overgrowth and increased bone density. Loss of function mutations of SOST gene, coding for sclerostin, are linked to sclerosteosis. Sclerostin plays a critical role inhibiting osteoblastic activity and preventing excessive bone formation by antagonizing the Wnt signaling pathway. Sclerosteosis patients are often tall and have excessive body weight due to high skeletal weight. To...

hrp0095p2-195 | Growth and Syndromes | ESPE2022

Syndromic Disorders with Short Stature

Zerrouki Dounia , Alla Achwak , Rami Imane , Derkaoui Nada , Benyekhlef Salma , Rouf Siham , Latrech Hanane

Keywords: Short stature, Noonan syndrome, Prader-Willi syndrome, Silver-Russell syndrome, genetic syndromesIntroduction: Short stature is one of the major components of dysmorphic syndromes. Growth failure may be due to a wide variety of mechanisms, either related to the growth hormone (GH)/insulin-like growth factor axis or to underlying unknown pathologies. At present, GH therapy is used in most syndromic disorders, al...