Cargando…

Cases Referred from the Turkish National Screening Program: Frequency of Congenital Hypothyroidism and Etiological Distribution

OBJECTIVE: The aim of this study was to evaluate cases referred from the congenital hypothyroidism (CH) newborn screening program. METHODS: Infants referred to Pediatric Endocrinology between 30.09.2015 - 01.04.2018 because of suspected CH identified by National Neonatal Screening Program were prosp...

Descripción completa

Detalles Bibliográficos
Autores principales:	Donbaloğlu, Zeynep, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Aycan, Zehra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745463/ https://www.ncbi.nlm.nih.gov/pubmed/30630811 http://dx.doi.org/10.4274/jcrpe.galenos.2019.2018.0255

Ejemplares similares

Effect of gonadotropin-releasing hormone analog treatment on final height in girls aged 6–10 years with central precocious and early puberty
por: Onat, Pınar Şimşek, et al.
Publicado: (2020)

What Has National Screening Program Changed in Cases with Congenital Hypothyroidism?
por: Özgelen, Şebnem, et al.
Publicado: (2014)

Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia
por: Bayramoğlu, Elvan, et al.
Publicado: (2021)

Evaluation of Gonadotropin Responses and Response Times According to Two Different Cut-Off Values in Luteinizing Hormone Releasing Hormone Stimulation Test in Girls
por: Özalkak, Şervan, et al.
Publicado: (2020)

Evaluation of Growth Hormone Results in Different Diagnosis and Trend Over 10 Year of Follow-up: A Single Center Experience
por: Aycan, Zehra, et al.
Publicado: (2021)

A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
por: Ceylan, Dilara, et al.
Publicado: (2021)

A case of prohormone convertase deficiency diagnosed with type 2 diabetes
por: Karacan Küçükali, Gülin, et al.
Publicado: (2021)

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
por: Keskin, Melikşah, et al.
Publicado: (2017)

Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience
por: Elmaoğulları, Selin, et al.
Publicado: (2021)

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
por: Aycan, Zehra, et al.
Publicado: (2018)

Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases
por: Yılmaz Ağladıoğlu, Sebahat, et al.
Publicado: (2013)

Antimüllerian Hormone Levels of Infants with Premature Thelarche
por: Muratoğlu Şahin, Nursel, et al.
Publicado: (2019)

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism
por: Şıklar, Zeynep, et al.
Publicado: (2012)

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

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make
por: Çetinkaya, Semra, et al.
Publicado: (2018)

Perinatal outcomes of high-dose vitamin D administration in the last trimester
por: Karacan Küçükali, Gülin, et al.
Publicado: (2021)

The Level of Inflammatory Markers and Their Relationship with Fat Tissue Distribution in Children with Obesity and Type 2 Diabetes Mellitus
por: Akalın Ertürk, Beyza, et al.
Publicado: (2023)

Hypothyroidism Due to Hepatic Hemangioendothelioma: A Case Report
por: Çetinkaya, Semra, et al.
Publicado: (2010)

Status of Central Precocious Puberty Cases at the Onset of Coronavirus Disease 2019 Pandemic: A Single-Center Experience
por: Orman, Burçe, et al.
Publicado: (2022)

Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children?
por: Karacan Küçükali, Gülin, et al.
Publicado: (2021)

Hemolytic Anemia due to Glucose 6 Phosphate Dehydrogenase Deficiency Triggered by Type 1 Diabetes Mellitus
por: Orman, Burçe, et al.
Publicado: (2023)

Eight-Year Follow-up of a Girl with McCune-Albright Syndrome
por: Aycan, Zehra, et al.
Publicado: (2011)

A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome
por: Peltek Kendirci, Havva Nur, et al.
Publicado: (2012)

Etiology of congenital hypothyroidism in Isfahan: Does it different?
por: Hashemipour, Mahin, et al.
Publicado: (2014)

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism
por: Aycan, Zehra, et al.
Publicado: (2017)

Does Congenital Hypothyroidism Have Different Etiologies in Iran?
por: Karamizadeh, Zohre, et al.
Publicado: (2011)

Timing of thyroid ultrasonography in the etiological investigation of congenital hypothyroidism
por: Borges, Maria de Fátima, et al.
Publicado: (2017)

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis
por: Savaş-Erdeve, Şenay, et al.
Publicado: (2011)

Subnormal Growth Velocity and Related Factors During GnRH Analog Therapy for Idiopathic Central Precocious Puberty
por: Muratoğlu Şahin, Nursel, et al.
Publicado: (2018)

Unfavorable Effects of Low-carbonhydrate Diet in a Pediatric Patient with Type 1 Diabetes Mellitus
por: Güleryüz, Ceren, et al.
Publicado: (2023)

Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review
por: Karacan Küçükali, Gülin, et al.
Publicado: (2021)

Demographic Features and Etiology of Congenital Hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016
por: Al Jafari, Mohammed, et al.
Publicado: (2020)

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)

Relationships Between Osteocalcin, Glucose Metabolism, and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?
por: Abseyi, Nilay, et al.
Publicado: (2012)

A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan
por: Nagasaki, Keisuke, et al.
Publicado: (2013)

Less known aspects of central hypothyroidism: Part 2 – Congenital etiologies
por: Benvenga, Salvatore, et al.
Publicado: (2018)

Serological Characteristics, Etiological Analysis, and Treatment Prognosis of Children with Congenital Hypothyroidism
por: shen, Lin, et al.
Publicado: (2022)

The Italian National Register of infants with congenital hypothyroidism: twenty years of surveillance and study of congenital hypothyroidism
por: Olivieri, Antonella
Publicado: (2009)

The Turkish Neonatal Society proposal for the management of COVID-19 in the neonatal intensive care unit
por: Erdeve, Ömer, et al.
Publicado: (2020)

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels
por: Şıklar, Zeynep, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_k84bnnie7q2dkarrlklf5ba4q9