hrp0082p3-d3-836 | Growth (2) | ESPE2014

What is the Profile of Gigantism: Seven Observations

Achir Samia , Semrouni Mourad

Background: Gigantism is a condition characterized by excessive growth and height significantly above average; it is usually caused by a tumor on the pituitary gland. In some cases the condition can be passed on genetically through a mutated gene.Objective and hypotheses: Describe clinical, hormonal, and morphological profile of seven children with gigantism. Mean age=14 years (9–16), age of onset of symptoms 12 years. Tall stature (50%), and brain ...

hrp0098p3-323 | Late Breaking | ESPE2024

Etiology and characteristics of children with short stature in endocrinology department

Azzoug Samira , Achir Samia

Growth retardation is frequent reason of consultation in endocrinology department.Its investigation is guided by weight and statural curves, as well as growth velocity, the breakage of which should alert us to an acquired tumoral pathology.The etiologies are grouped into pathological and common etiologies.We report the results of study of 156 children presenting with short stature in the endocrinology department of Beni Messous where we found that the proportion of boys to gir...

hrp0082p3-d3-916 | Pituitary (1) | ESPE2014

Polyuria Syndrome Associated with Visual Disorders in Children: Discuss at First Craniopharyngioma, the Primary Polydypsia is an Exclusion Diagnosis

Yacine Rahem , Merouane Belacel , Samia Achir

Background: True diabetes insipidus (DI) is a rare disease in children, defined as the excretion of hypotonic urine and polydypsia, secondary to an absolute or relative deficiency of antidiuretic hormone arginine vasopressin (central DI) or a resistance to the action of this hormone (nephrogenic DI). To differentiate from primary polydypsia.Objective and hypotheses: We report the case of AM a 13 years old girl, with personal history of cholecystectomy at...

hrp0098p3-172 | Growth and Syndromes | ESPE2024

Noonan syndrome: case report of 4 patients

Mokrane Amel , Azzoug Samira , Achir Samia

Introduction: Noonan syndrome (NS) is a rare autosomal dominant genetic disorder with an estimated incidence of 1/2500. Diagnosis is mainly clinical, with the association of dysmorphic signs, cardiac malformations and delayed growth.Observation: The cases involved 2 boys and 2 girls. The average age at diagnosis was 9.5 years, with a characteristic facial dysmorphia in 100% of cases, cardiac malformations such as pulmona...

hrp0082p3-d3-915 | Pituitary (1) | ESPE2014

Thickened Pituitary Stalk with Central Diabetes Insipidus: What Diagnosis?

Merazka Amel , Samia Achir , Ouidad Baz , Dalila Foudil , Mourad Semrouni

Background: Central diabetes insipidus (DIC) is usually the final result of lesions affecting the hypothalamic–neurohypophyseal system, for the children, germinoma is the main reason. The MRI aspect is often limited to thickness pituitary stalk with loss of hyperintensity of the neurohypophysis.Objective and hypotheses: Thickening of pituitary stalk is suggestive of germinoma, the clinical picture is dominated by a DIC (90%), associated to hypopitui...

hrp0094p2-366 | Pituitary, neuroendocrinology and puberty | ESPE2021

Hypothalamic obesity in children with craniopharyngioma

Baz Ouidad , Achir Samia , Tazibt Oulebsir , Mimouni Safia ,

Introduction: Lesional hypothalamic obesity is most frequently attributable to craniopharyngiomas. The aim of our work is to describe the modalities of occurrence of this complication in a series of 27 children with craniopharyngioma followed in our center. We carried out a descriptive retrospective study of 27 cases of craniopharyngioma in children followed in the endocrinology department of the CPMC over a period of 16 years.Re...

hrp0097p2-201 | GH and IGFs | ESPE2023

Etiology and characteristics of children with short stature in endpcrinology department

Azzoug Samira , Adimi Amel , Medjani Rania , Djouadi Anes , Sadira Nesserine , Achir Samia

Objectives: childhood growth influences their social and psychological behavior, and abnormal growth may reflect underlying pathological etiologies. We aim to study etiologies and carachteristics of short stature in children in endocrinology department.Methods: 160 children ranging from 2 years to 21 years with short stature were retrospectively studied.Results: In this study, a di...