hrp0092p2-216 | Multisystem Endocrine Disorders | ESPE2019

Hypothyroidism in a Two and a Half Year-Old Boy with an Angelman Syndrome (AS)

Janchevska Aleksandra , Bozinovski Georgi , Jordanova Olivera , Tasic Velibor , Gucev Zoran

Introduction: Angelman syndrome is caused by de novo maternal deletions in 15q11-q13 region of chromosome 15 in approximately 70% of affected children.Patient and Methods: A two and a half year-old boy with hypotonia, absence of speech, low weight (-4.38 SDS) and short stature (-1.14 SDS) had pale skin and typical facial features with wide and prominent forehead, low-lying ears, wide mouth, small and widely spaced te...

hrp0095p2-227 | Pituitary, Neuroendocrinology and Puberty | ESPE2022

Growth Hormone Deficiency in A Boy with Duplication 5q35.2q35.3

Janchevska Aleksandra , Plasheska-Karanfilska Dijana , Jordanova Olivera , Beqiri-Jashari Ardiana , Tasic Velibor , Gucev Zoran

Introduction: The genomic disorders caused by rearrangements in region 5q35, including the NSD1 (nuclear receptor SET domain containing protein-1) gene have various phenotypes depending on presence of deletions, duplications or inversions. Patients carrying microduplication have microcephaly, short stature, and mild to moderate intellectual delay or learning disability.Patients and methods: A six-year-old boy wa...

hrp0089p2-p221 | GH & IGFs P2 | ESPE2018

Growth Hormone Treatment in Children Born Small for Gestational Age (SGA)

Janchevska Aleksandra , Krstevska-Konstantinova Marina , Jordanova Olivera , Tasevska-Rmush Liljana , Tasic Velibor , Gucev Zoran

Introduction: Growth failure is a common consequence in small for gestational age (SGA) children.Patients and methods: The growth patterns and serum insulin like growth factor 1 (IGF1) concentrations before and after the 1st year under GH treatment of 32 short stature SGA born children have been evaluated. In addition, we investigated the insulin like growth factor 1 receptor (IGF1R) exon 2 as a hotspot for IGF1R genetic alterations. It is of note that n...

hrp0097p2-217 | Adrenals and HPA Axis | ESPE2023

Primary hypoaldosteronism due to aldosterone synthase deficiency in a small for gestational age born infant

Janchevska Aleksandra , Tasic Velibor , Antonievska Simona , Bujarovska Ivana , Iliev Blagorodna , Daniloski Darko , Jordanova Olivera , Gucev Zoran , Plaseska-Karanfilska Dijana

Key words: Primary hypoaldosteronism, aldosterone synthase deficiency, salt-wasting, failure to thrive, CYP11B2 gene mutationIntroduction: Aldosterone synthase deficiency is a rare autosomal recessive inherited disorder. The patients carry mutations in the CYP11B2 gene. It is primary hypoaldosteronism presented in early childhood with electrolyte abnormalities (hyponatremia, hyperkalemia, and metabolic ...

hrp0098p2-203 | Multisystem Endocrine Disorders | ESPE2024

Hyperthyroidism and type 1 diabetes mellitus in a girl with down syndrome

Sapundzija Felina , Sandeva Dragana , Beadini Narcize , Nonkulovski Danilo , Naunova Timovska Silvana , Jordanova Olivera , Abazi Nora , Janchevska Aleksandra

Introduction: Autoimmune endocrinopathies are associated with Down syndrome (DS), especially in pubertal female patients. Coexistence of hyperthyroidism and insulin-dependent diabetes mellitus (IDDM) is very rare in patients with DS. But, the possibility of their occurrence emphasizes the importance of annual screening.Patient and methods: An 11-year-old girl with Trisomy 21 (DS), BMI=20,7 kg/m2 and BMI z scor...