The Turkish Journal of Pediatrics
Smilar Issues: 121 Record Found
Surgical outcome of congenital valvar aortic stenosis
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Physiotherapy results in a baby with congenital lymphedema: a follow-up study
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Congenital cardiac defects with 22q11 deletion
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Clinical analysis of the trigger thumb of childhood
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Endobronchial stenting in a two-month-old infant with
bronchial compression secondary to tetralogy of Fallot and
absent pulmonary valve
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Triple-X syndrome accompanied by congenital adrenal hyperplasia: case report
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Congenital aneurysm of the muscular interventricular septum in a child
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Subacute sclerosing panencephalitis (SSPE) associated with congenital measles infection
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Noncardiac malformations in congenital heart disease: A retrospective analysis of 305 pediatric autopsies
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Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome
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Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment Case report
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An anencephalic monocephalus diprosopus “headed twin”: postmortem and CT findings with emphasis on the cranial bones
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Prenatal echocardiographic diagnosis of congenital heart disease: comparison of past and current results
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The triad of nesidioblastosis, congenital neuroblastoma and glomerulocystic disease of the newborn: a case report
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A rare cause of anemia and thrombocytopenia in a newborn: congenital malaria
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Chromosomal abnormalities in 457 Turkish patients with MCA/MR
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Plexiform neurofibroma of the tongue: a case report of a child
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Bilateral cervical chondrocutaneous remnants: a case report and review of the literature
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Prevalence and distribution of children with congenital heart diseases in the central Anatolian region, Turkey
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Dorfman-Chanarin syndrome: a case with hyperlipidemia
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Hypocalcemic seizure due to congenital rickets in the first day of life
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Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract
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Application of medical genetics in Turkey
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Correlation between vascular endothelial growth factor and leptin in children with cyanotic congenital heart disease
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A vanishing tongue-base cyst
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Report of three cases: congenital chylothorax and treatment modalities
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The Incidence of Congenital Malformations in Children with Cancer
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Double Outlet Right Ventricle with Giant Pulmonary Artery
Aneurysm and Severe Aortic Coarctation: Diagnosis with
Multislice CT
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Kabuki make-up syndrome with unilateral renal agenesis
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A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II
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A report of a patient with duplication of 7p13→pter and deletion of 2p23→pter due to a maternal 2p;7p translocation
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Early congenital syphilis with isolated bone involvement: a case report
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Endovascular stent implantation for coarctation of the aorta in children and young adults: intermediate follow-up results from Turkey
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Acute gastric volvulus due to congenital bands in a newborn case
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Modification of the endoscopic management of congenital duodenal stenosis
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Intraosseous Noninvoluting Congenital Hemangioma of the Mandible in a Neonate
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Final height of patients with classical congenital adrenal hyperplasia
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3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures
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HAX1 mutation in an infant with severe congenital neutropenia
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Congenital Nasolacrimal Duct Mucocele – A Case Report
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Tympanic Membrane Cholesteatoma: A Rare Finding
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Growth Hormone Deficiency Due to Traumatic Brain Injury in a Patient with X-linked Congenital Adrenal Hypoplasia
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Congenital Pulmonary Fibrosarcoma in a Newborn with Hypoglycemia and Respiratory Distress: Case Report
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An Uncommon Cause of Neonatal Respiratory Distress
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Is Basal Serum 17-OH Progesterone A Reliable Parameter To Predict Nonclassical Congenital Adrenal Hyperplasia in Premature Adrenarche?
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Prenatally Detected Congenital Cystic Adenomatoid Malformation and Postnatally Diagnosed Trisomy 13: Case Report and Review Of The Literature
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Prenatally Diagnosed Case of 22q11.2 Deletion Syndrome Associated with Pulmonary Artery Aneurysm
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Congenital Distal Esophageal Obstruction Caused by Intraluminal Mucosal Web
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Malignant melanoma developed on a congenital melanocytic nevus with lymph node metastasis in a 19-month-old boy
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Congenital Central Hypoventilation Syndrome with Hirschsprung’s Disease due to PHOX2B Gene Mutation in a Turkish Infant
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Congenital Hypothyroidism Screening Program in Turkey: A Local Evaluation
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Bart’s Syndrome Associated with Pyloric and Choanal Atresia
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Bullous Skin Lesions in a Jaundiced Infant after Phototherapy: A Case of Congenital Erythropoietic Porphyria
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Oral Findings and Clinical Implications of Patients with Congenital Neutropenia: A Literature Review
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Monitoring and Prognostic Evaluation of Patients with Congenital Hypothyroidism Treated in a Pediatric Endocrinology Unit
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Generalized periosteal reaction and tissue swelling secondary to prolonged prostaglandin E1 infusion and venous stasis: a case report
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Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectra
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Congenital epulis: from birth to childhood
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Uncommon congenital antral web misdiagnosed twice as a pyloric ulcer: successful treatment with endoscopic balloon dilatation
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Atypical Fryns syndrome: clinical, radiological and pathological findings
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Congenital Mucocele of the Tongue: A Case Report and Review of the Literature
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A Report of Adenocarcinoma In Situ and Congenital Pulmonary Airway Malformation in a Three-Day-Old Infant with a Review of the Literature
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Congenital Hairy Polyp and Autoamputation in an Infant with Acute Otitis Media
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Hearing Stimulation of the Pediatric Patient with Congenital Aural Atresia: Surgical and Audiological Evaluation of 38 Patients
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A Rare Cause of Congenital Diarrhea in a Turkish Newborn: Tufting Enteropathy
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Neonate Born to Hepatitis B Carrier Mother Presenting with Congenital Onychodysplasia of the Index Finger (Iso–Kikuchi Syndrome)
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Bilateral Congenital Cataracts in an Infant with Klinefelter Syndrome
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A Newborn with Pertussis Accompanying Nephrotic Syndrome
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Ectopic Salivary Gland of the Base of the Tongue: A Rare Cause of Neonatal Respiratory Distress
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A congenital proximal tracheoesophageal fistula 14 years after surgical repair of esophageal atresia with distal tracheoesophageal fistula
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Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue
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Acute respiratory distress for late-presenting congenital diaphragmatic hernia
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Novel Nonsense Mutation of GPC3 Gene in a Patient with Simpson-Golabi-Behmel Syndrome
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Postoperative chylous ascites: increased scrotal volume as "alarm bell"
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Three Cases of a Rare Disease, Congenital Chloride Diarrhea, Summons Up the Variation in the Clinical Course and Significance of Early Diagnosis and Adequate Treatment in the Prevention of Intellectual Disability
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Association between genotype, clinical presentation, and severity of congenital adrenal hyperplasia: a review
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Prematurity due to Maternal Brucella Infection and Review of the Literature
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A Girl with Steroid Cell Ovarian Tumor Misdiagnosed as Non-Classical Congenital Adrenal Hyperplasia
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Postmortem Clinical Examination by Experienced Clinical Geneticists as an Alternative to Conventional Autopsy for Assessment of Fetal and Perinatal Deaths in Countries with Limited Resources
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Report of a Case of Neonatal Chylothorax That Responded to Long-Term Octreotide Treatment, and Review of the Literature
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Intralobar Pulmonary Sequestration Associated with Congenital Broncho-Esophageal Fistula
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Late presentation of congenital diaphragmatic hernia
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Congenital malaria: Importance of diagnosis and treatment in pregnancy
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Recessive congenital methemoglobinemia in immediate generations
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Comparison of risk scoring systems in congenital heart surgery
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A congenital soft tissue Ewing sarcoma in a newborn patient
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Congenital insensitivity to pain: How should anesthesia be managed?
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Kocuria kristinae-caused sepsis in an infant with congenital tufting enteropathy
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Isolated thoracoschisis: Case report
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Congenital heart defects in Williams syndrome
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Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2
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Comparison of risk factors in newborn hearing screening in a developing country
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Nutritional rehabilitation for children with congenital heart disease with left to right shunt
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Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis
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A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy
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Foot hexadactyly, social implications and management in the African setting: Case report
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Perioperative factors associated with hyperglycemia after pediatric cardiac surgery and impact of hyperglycemia on morbidity and mortality
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Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center
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Is serum procalcitonin level a reliable indicator in early diagnosis of congenital pneumonia?
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Asymptomatic giant congenital left atrial aneurysm
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Fanconi anemia: a single center experience of a large cohort
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Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism
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Cigarette smoking in adolescents with type 1 diabetes mellitus and congenital adrenal hyperplasia
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Cranial MR characteristics of Cerebral Palsy cases and correlation of findings with clinical results
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Novel mutation and severe respiratory failure in congenital disorders of glycosylation Type Ix
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Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy
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Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia
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A rare case of syndromic severe congenital neutropenia: JAGN1 mutation
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Effect of long-term glucocorticoid therapy on bone mineral density of the patients with congenital adrenal hyperplasia
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Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene
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Congenital esophageal diverticulum in a very low birth weight infant: case report and review of literature
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Awareness assessment for parents of children with congenital heart diseases regarding fetal echocardiography
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Giant ethmoidal mucocele leading to proptosis and hypertelorism in a pediatric patient with cystic fibrosis: a case report
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Pacemaker lead-induced tricuspid stenosis treated with percutaneous valvotomy
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Clinical and demographic characteristics of childhood neuro-ophthalmology diseases at a tertiary eye care center
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Early-auditory intervention in children with hearing loss and neurodevelopmental outcomes: cognitive, motor and language development
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A case of juvenile systemic sclerosis and congenital pulmonary airway malformation related mucinous adenocarcinoma of the lung: paraneoplastic syndrome or just a coincidence?
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A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
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Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I
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Evaluation of the relationship between cardiopulmonary exercise test findings and clinical status in children and adolescents with congenital heart disease
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Prenatal diagnosis of congenital megalourethra: case report and literature review
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