Cargando…

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

OBJECTIVE: Monogenic diabetes is a heterogeneous disease that causes functional problems in pancreatic beta cells and hyperglycemia. The aim of this study was to determine the clinical and laboratory features, the admission characteristics and distribution of monogenic form of diabetes in childhood...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gökşen, Damla, Yeşilkaya, Ediz, Özen, Samim, Kor, Yılmaz, Eren, Erdal, Korkmaz, Özlem, Berberoğlu, Merih, Karagüzel, Gülay, Er, Eren, Abacı, Ayhan, Evliyaoğlu, Olcay, Akbaş, Emine Demet, Ünal, Edip, Bolu, Semih, Nalbantoğlu, Özlem, Anık, Ahmet, Tayfun, Meltem, Büyükinan, Muammer, Abalı, Saygın, Can Yılmaz, Gülay, Kör, Deniz, Söbü, Elif, Şıklar, Zeynep, Polat, Recep, Darcan, Şükran
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2021
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638634/ https://www.ncbi.nlm.nih.gov/pubmed/34250910 http://dx.doi.org/10.4274/jcrpe.galenos.2021.2021.0056

Ejemplares similares

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study
por: Şıklar, Zeynep, et al.
Publicado: (2016)

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
por: Şıklar, Zeynep, et al.
Publicado: (2020)

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study
por: Şimşek, Damla Gökşen, et al.
Publicado: (2013)

Serum IGF-1 and IGFBP-3 Levels in Healthy Children Between 0 and 6 Years of Age
por: Yüksel, Bilgin, et al.
Publicado: (2011)

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study
por: Berberoğlu, Merih, et al.
Publicado: (2008)

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome
por: Dağdeviren Çakır, Aydilek, et al.
Publicado: (2021)

The Gonadotropin-Releasing Hormone Analogue Therapy May Not Impact Final Height in Precocious Puberty of Girls With Onset of Puberty Aged 6 - 8 Years
por: Korkmaz, Ozlem, et al.
Publicado: (2019)

Correction to: The Gonadotropin-Releasing Hormone Analogue Therapy May Not Impact Final Height in Precocious Puberty of Girls With Onset of Puberty Aged 6 - 8 Years
por: Korkmaz, Ozlem, et al.
Publicado: (2019)

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis
por: Ergür, Ayça Törel, et al.
Publicado: (2011)

Long−Term Follow−Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5
por: Erdeve, Şenay Savaş, et al.
Publicado: (2010)

Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience
por: Esen, İhsan, et al.
Publicado: (2019)

Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children
por: Akduman, Filiz, et al.
Publicado: (2022)

Syndromic Disorders with Short Stature
por: Şıklar, Zeynep, et al.
Publicado: (2014)

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey
por: Şıklar, Zeynep, et al.
Publicado: (2016)

Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up
por: Öcal, Gönül, et al.
Publicado: (2008)

Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene
por: Özen, Samim, et al.
Publicado: (2020)

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
por: Yeşilkaya, Ediz, et al.
Publicado: (2015)

Two Siblings with Isolated GH Deficiency Due to Loss−of−Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation
por: Şıklar, Zeynep, et al.
Publicado: (2010)

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
por: Savaş-Erdeve, Şenay, et al.
Publicado: (2021)

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?
por: Çamtosun, Emine, et al.
Publicado: (2018)

Effectiveness of Continuous Subcutaneous Insulin Infusion Pump Therapy During Five Years of Treatment on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
por: Korkmaz, Özlem, et al.
Publicado: (2018)

In response to: “Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic”
por: Cimbek, Emine Ayça, et al.
Publicado: (2022)

The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases
por: Evin, Ferda, et al.
Publicado: (2021)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
por: Darendeliler, Feyza, et al.
Publicado: (2015)

Prevalence of Obesity and Metabolic Syndrome in Children with Type 1 Diabetes: A Comparative Assessment Based on Criteria Established by the International Diabetes Federation, World Health Organisation and National Cholesterol Education Program
por: Yayıcı Köken, Özlem, et al.
Publicado: (2020)

A Rare Cause of Recurrent Acute Pancreatitis in a Child: Isovaleric Acidemia with Novel Mutation
por: Sag, Elif, et al.
Publicado: (2017)

Combined Evaluation of IGF−1 and IGFBP−3 as an Index of Efficacy and Safety in Growth Hormone Treated Patients
por: Şıklar, Zeynep, et al.
Publicado: (2009)

Childhood Sustained Hypercalcemia: A Diagnostic Challenge
por: Çullas İlarslan, Nisa Eda, et al.
Publicado: (2017)

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia
por: Çetin, Tuğba, et al.
Publicado: (2018)

The Effectiveness of Sirolimus Treatment in Two Rare Disorders with Nonketotic Hypoinsulinemic Hypoglycemia: The Role of mTOR Pathway
por: Şıklar, Zeynep, et al.
Publicado: (2020)

Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment
por: Kontbay, Tuğba, et al.
Publicado: (2022)

Renal Anomalies Associated with Ectopic Neurohypophysis
por: Özen, Samim, et al.
Publicado: (2011)

Clinical Course of Hashimoto's Thyroiditis and Effects of Levothyroxine Therapy on the Clinical Course of the Disease in Children and Adolescents
por: Özen, Samim, et al.
Publicado: (2011)

A Randomized Clinical Trial Comparing Breakfast and Bedtime Administration of Insulin Glargine in Children and Adolescents with Type 1 Diabetes
por: Gökşen Şimşek, Damla, et al.
Publicado: (2008)

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
por: Eren, Erdal, et al.
Publicado: (2019)

A Long-Term Comparison of Presenting Characteristics of Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic
por: Kaya, Gülay, et al.
Publicado: (2022)

Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation
por: Korkmaz, Özlem, et al.
Publicado: (2017)

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results
por: Ergür, Ayça Törel, et al.
Publicado: (2010)

Trends in the Frequency of HLA DR-DQ Haplotypes Among Children and Adolescents with Type 1 Diabetes Mellitus in the Southeast Region of Turkey
por: Keskin, Mehmet, et al.
Publicado: (2012)

Ghrelin Levels in Children with Constitutional Delay of Growth and Puberty
por: Şen, Tolta Altuğ, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_6hddm8nu1qftmdqm71f20co5fa