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Toplam kayıt 17, listelenen: 1-17
Oral Health Status In Patients With Mucopolysaccharidoses
(Turkish J Pediatrics, 2018)
The aim of this study is to assess oral clinical and radiological findings of patients with mucopolysaccharidoses (MPS) which are a group of rare inherited disorders of glycosaminoglycan catabolism. In this retrospective ...
Meconium Periorchitis: An Incidentally Diagnosed Rare Entity During Inguinal Herniorraphy
(Turkish J Pediatrics, 2018)
Meconium periorchitis (MPO) is a rare disorder caused by meconium peritonitis with the leakage of meconium into the scrotal sac through the patent processus vaginalis. MPO may be rarely detected during inguinal hernia ...
Changes Of Primary Headache Related White Matter Lesions In Pediatric Patients
(Turkish J Pediatrics, 2018)
We aimed to describe the long-term prognosis of white matter lesions detected on magnetic resonance imaging in children with primary headache. Children who were admitted with the complaint of headache and had nonspecific ...
Advantage of the Subcutaneous Immunoglobulin Replacement Therapy in Primary Immunodeficient Patients With or Without Secondary Protein Loss
(Turkish J Pediatrics, 2018)
In recent years subcutaneous immunoglobulin is widely used for primary immunodeficient patients. Subcutaneous administration provides a more stable and higher serum immunoglobulin levels due to continuous and steady ...
Evaluation Of Psychological Characteristics Of Turkish Children With Type 1 Diabetes Mellitus From Two Demographically And Geographically Distinct Regions
(Turkish J Pediatrics, 2018)
Type 1 diabetes mellitus (T1DM), patients have an increased risk of psychiatric morbidity compared to their healthy counterparts. The aim of the present study is to evaluate the demographic and laboratory data and psychological ...
Anauxetic Dysplasia: A Rare Clinical Entity
(Turkish J Pediatrics, 2018)
Cartilage hair hypoplasia and anauxetic dysplasia spectrum constitute a group of autosomal recessive disorders characterized by variable extent of metaphyseal to spondylometaepiphyseal involvement and various additional ...
Does Inhaled Salbutamol Before Surfactant Therapy Have Any Beneficial Effect?
(Turkish J Pediatrics, 2018)
Beta (beta)(2) adrenergic receptors are present in alveolar type II cells. Previously, the beneficial effects of inhaled salbutamol treatment on respiratory outcomes were shown in premature infants with transient tachypnea ...
Home Accident Or Physical Abuse: Evaluation Of Younger Children Presenting With Trauma, Burn And Poisoning In The Pediatric Emergency Department
(Turkish J Pediatrics, 2018)
Most cases of physical abuse and neglect refer to pediatric emergency clinics, and these patients are diagnosed as only home accidents. Cases that cannot be diagnosed and managed correctly are again exposed to severe trauma ...
Epigenotype And Phenotype Correlations In Patients With Beckwith-Wiedemann Syndrome
(Turkish J Pediatrics, 2018)
Beckwith-Wiedemann Syndrome (BWS) is one of the most common overgrowth syndromes. Cancer predisposition is an important feature of this clinically heterogeneous syndrome. Patients may have fetal and early childhood overgrowth, ...
Cognitive And Behavioral Impairment In Mild Hyperphenylalaninemia
(Turkish J Pediatrics, 2018)
As elevated phenylalanine (Phe) is detrimental to brain functions, determining a safe upper limit of blood Phe is important for initiation of treatment plans and setting Phe targets in hyperphenlalaninemic patients. It is ...
Perfusion Index and Pleth Variability Index in the First Hour of Life According to Mode of Delivery
(Turkish J Pediatrics, 2018)
Perfusion index (PI) is a relative assessment of the pulse strength at the monitoring site. The plethysmographic variability index (PVI, pleth variability index) is a noninvasive and continuous measure of the dynamic change ...
A Patient Heterozygous for R92Q Mutation with Periodic Fever and Aphthous Stomatitis, Pharyngitis, and Adenitis (Pfapa) Syndrome-Like Phenotype
(Turkish J Pediatrics, 2018)
Tumor necrosis factor receptor associated periodic syndrome (TRAPS) is an autosomal dominant disease caused by mutations located on the type 1 tumor necrosis factor receptor (TNFRSF1A) gene. Here we present a 3-year-old ...
Pulmonary Thromboendarterectomy in Pediatric Patients: Report of Three Cases
(Turkish J Pediatrics, 2018)
Chronic thromboembolic pulmonary hypertension (CTEPH), which occurs due to impartial resolution of the pulmonary thrombus, is a rare type of pulmonary hypertension. However, most patients have an excellent long-term survival ...
Non-Immune Hydrops Fetalis: A Retrospective Analysis Of 151 Autopsies Performed At A Single Center
(Turkish J Pediatrics, 2018)
We retrospectively evaluated autopsies performed on 151 non-immune hydrops fetalis (NIHF) cases to determine the etiology and pathological findings. Further, cases identified between 1980 and 2004 were compared with those ...
Speech Delay In Toddlers: Are They Only "Late Talkers"?
(Turkish J Pediatrics, 2018)
Speech delay is prevalent in toddlers. Although some children with speech delay are able to catch up with their peers with time, the delay might be part of a broader condition such as global developmental delay, which ...
Outcome Of Out-Of-Hospital Cardiopulmonary Arrest In Children: A Multicenter Cohort Study
(Turkish J Pediatrics, 2018)
The aim of this study was to evaluate the demographic characteristics of children who experienced out-of-hospital cardiopulmonary arrest (CPA), and to assess the impact of the bystander cardiopulmonary resuscitation (CPR) ...
Prevalence and Seasonal Distribution of Viral Etiology of Respiratory Tract Infections in Inpatients and Outpatients of the Pediatric Population: 10 Year Follow-Up
(Turkish J Pediatrics, 2018)
The aim of this study was to investigate the prevalence and seasonal distribution of respiratory viruses in pediatric patients. Nasopharyngeal swab specimens, demographic and clinical information were collected from 1240 ...