hrp0089p3-p104 | Diabetes & Insulin P3 | ESPE2018

The Frequency of Diabetic Ketoacidosis Hospitalization in Siberian Children and Adolescent

Osokina Irina

Introduction: Diabetic ketoacidosis is a frequent reason for hospital admission of children with newly diagnosed diabetes and the most frequent cause for hospitalization of children with poorly controlled diabetes.Aim: To evaluate the frequency of diabetic ketoacidosis (DKA) hospitalization for pediatric patients and resources for its decrease.Methods: Subjects included children <19 years who hospitalized with DKA in the pediat...

hrp0089p3-p304 | Pituitary, Neuroendocrinology and Puberty P3 | ESPE2018

A 2-Year-Old Boy with Epiphysis Tumor and Precocious Puberty

Osokina Irina

Epiphysis inhibits formation and secretion of the most pituitary hormones and at the first turn gonadotropins. Frequency of epiphysis tumors, pinealomas in children is 2.5% of all verified tumors of brain. 75% of epiphysis tumors are malignant. Endocrinological disturbances can be the first signs of pinealoma. In 10% cases there is precocious puberty syndrome. A 2.5 year-old boy presented to the endocrinology department with an 16-month history of accelerated physical developm...

hrp0089p3-p305 | Pituitary, Neuroendocrinology and Puberty P3 | ESPE2018

Central Precocious Puberty as a Result of Hypotalamus Hamartoma

Osokina Irina

Presentation of case: A 3-year-old boy with central precocious puberty as a result of the organic lesion of brain (hamartoma of hypotalamus). Complains.Increased height velocity, masculinization, fast growth of external genitalia, frequent erections, acne, low voice. Medical history. The baby was born with weight 3400 g. The age of the mother at birth of the child was 23 years. The breast feeding 6 months. In the age of 24 months boy started to grow very fastly. In the age of ...

hrp0089p3-p306 | Pituitary, Neuroendocrinology and Puberty P3 | ESPE2018

Precocious Puberty as a Result of Ectopic Hormone-Producing Tumor

Osokina Irina

Ectopic hormone products are typical for cancerous cells. Cancerous cells can produce ACTH, lipotropin, alfa-melanocytostimulating hormone, beta-endorfin, vasopressin, oxytocin, insuline, glucagon, gastrin, secretin, VIP, calcitonin, hypothalamic releasing-hormones, prolactin, parathyroid hormone, growth hormone, chorionic gonadotropin, growth factors. In the majority of ectopic hormone-producing tumor cases clinical symptoms are absent. This is explained by the fact that tumo...

hrp0094p2-483 | Thyroid | ESPE2021

A 9-year-old girl with Van Wyk and Grumbach syndrome: precocious puberty as a rare consequence of hypothyroidism

Osokina Irina

Background: The syndrome consisting of primary hypothyroidism, precocious puberty, and massive ovarian cysts was termed Van Wyk and Grumbach syndrome (VWGS) in 1960. Chronic lymphocytic thyroiditis is the more common cause of hypothyroidism in children. In patients with severe longstanding hypothyroidism, the sella turcica may be enlarged due to thyrotrope hyperplasia. Puberty tends to be delayed in hypothyroid children in proportion to the retardation in the bone age, althoug...

hrp0094p2-484 | Thyroid | ESPE2021

Iodine Deficiency Cretinism in Tuva Republic

Osokina Irina

Introduction: Iodine deficiency is the most common cause of mental retardation that can be prevented. The most serious consequence of iodine deficiency is cretinism. The Republic of Tuva is one of 89 administrative territories of the Russian Federation. Tuva lies in the south of Siberia and bordering Mongolia. In 1997 we first discovered the pocket of severe iodine deficiency in the Republic of Tuva and found cases of endemic cretinism. The aim: To study the features of iodine...

hrp0094p2-488 | Thyroid | ESPE2021

The state of iodine deficiency in Krasnoyarsk territory according to results of neonatal TSH screening in 2019

Osokina Irina

Background: Iodine deficiency is associated with goiter and impaired brain function. Neonatal thyroid-stimulating hormone (TSH) screening for congenital hypothyroidism used as an indicator of the degree of iodine deficiency. In the absence of iodine deficiency, the frequency of neonatal TSH above 5 mU/L whole blood is less than 3%. A frequency of 3%-19.9% indicates mild IDD. Frequencies of 20%-39.9% indicate moderate and above 40% severe IDD.The aim: to ...

hrp0084p3-888 | Fat | ESPE2015

Weight and the Factors Influencing it in a Cohort of School Aged Children

Pop Raluca , Capraru Oana , Pascanu Ionela

Background: Weight disturbances in children are an important problem, both underweight and obesity having important health consequences. There is an ongoing debate about their cause, the risk factors involved and the need for public health policies focused on their prevention.Objective and hypotheses: The aim of this study was to estimate the prevalence of weight disturbances in a cohort of school-aged children and to analyse some factors considered to p...

hrp0084p3-1097 | Perinatal | ESPE2015

Experience in Insulin Pump Therapy in the Treatment of Neonatal Diabetes

Asiet Tlif , Irina Chernyak , Irina Shtoda , Irina Golovenko , Elena Kondratyeva

Background: Neonatal diabetes (ND) at first 6 months and its frequency is one in 500 000 newborns. There are some difficulties in its treatment, due to low demand and high sensitivity to insulin.Case presentation: We present the experience in insulin pump therapy treatment. A 13 days girl was taken to Regional Children’s Clinical Hospital in Krasnodar. It was the child from the1st pregnancy with toxicosis in the one st trimester, threat of terminati...

hrp0092p3-234 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2019

Diagnostic Dilemma in a 46 XY Female

Waldner Richelle , Rosolowsky Elizabeth , Caluseriu Oana , Grimbly Chelsey

Introduction: Disorders of sex development (DSD) are conditions with discrepancies between the chromosomal, gonadal, and phenotypic sex. We present a case of a phenotypic 46 XY female with primary amenorrhea and full thelarche, presence of Mullerian structures, elevated testosterone with no virilization, and bilateral adnexal masses. Our differential diagnosis included Androgen Insensitivity and Gonadal Dysgenesis.Case Descriptio...