Articles on yenidoğan

MUSTAFA ÖZ, NURİYE EMİROĞLU

2026, Vol 42, Issue 2, Page 101-107

Objective: Congenital malformations (CM) constitute one of the most important causes of neonatal and childhood deaths, chronic diseases and morbidity. This study aimed to identify CM, determine their frequency and investigate the factors that may be effective in etiology in patients treated in the...

SAİME SÜNDÜS UYGUN, FATMA ÖZCAN SIKI

2025, Vol 41, Issue 4, Page 201-204

Objective: This study aims to compare the guideline compliance of two widely used AI-based chatbot systems, ChatGPT and Bing AI, with the clinical recommendations outlined in the Disorders of Sex Development (DSD) guideline published by the Turkish Neonatal Society. Materials and Methods: A...

SAİM AÇIKGÖZOĞLU, HASAN KOÇ, MUSTAFA ERKEN, RECEP MEMİK, MEHMET EMİN SAKARYA

1991, Vol 7, Issue 2, Page 121-125

Real dine ultrasonography is succesfully employed to determine hip position in infancy. It also offers an alternative method for evaluating ac.-etabular depelopınent. The hips of 55 infant with normal clinical hip signs were examined by U.S. in the coronal lateral US scan. acetabular,...

MEHMET KIYAN, LÜGEN CENGIZ, TEVFIK CENGIZ, FADIL KARA, M. ŞAHIN UĞUREL, HAKAN LEBLEBICIOĞLU

1992, Vol 8, Issue 4, Page 573-577

In this study, IISV-1 IgG and 1gM were detected by elisa iır the sera of 73 mothers having obstetrical pathologies and in 73 newborns' sera. In mothers' sera IISV-1 IgG was found to be 7/73 (9.6 %) and HSV-1 1RM was 71173 (97.3 %) seropositive. In 26- 40 age group of all 34 cases IISV-1 IgG was...

MEHMET ALİ MALAS, ERKAN ATAŞ

1999, Vol 15, Issue 2, Page 79-82

The aim of this study was to examine vvhether low birth weight has a relation with the physical values of foot size among nevvborns. This study was performed on 60 lovv birth vveight nevvborn infants (30 males and 30 females) and 60 normal healty nevvborns (30 males and 30 females). Bimalleolus...

HASAN KOÇ, PAKIZE DEMIREZICI, İSMAIL REISLI, SAİM AÇIKGÖZOĞLU

2000, Vol 16, Issue 1, Page 59-63

Osteogenesis imperfecta which is a heritable connective tissue disorder characterized by increased bone fragility and frequent bone fractures. The Cardinal symptom pathologic fracture which is often recognized before birth: blue sclera and deafness may be present. İn this paper, three nevvborn were...

MEHMET ALİ MALAS, ERKAN ATAŞ

2002, Vol 18, Issue 4, Page 227-234

Purpose: İn this study, we aimed to determine the measurements and the relation betvveen craniofacial morpho- logy and orbita in full term, prematüre nevvborns and nevvborn with low birth vveight. Materials and method: We vvere studied 60 prematüre nevvborns (Male 30, Female 30) who vvere aged...

OSMAN BAŞPINAR, BILGE KUTLUHAN AKSU, GÜNER KARATEKIN, ASIYE NUHOĞLU

2002, Vol 18, Issue 4, Page 235-239

Classic kernicterus or the neurotoxicity of neonatal hyperbilirubinemia is known well, but the pathological jaundice may show itself vary different subtle neurological dysfunction at the some patients. 159 patients male 61.1 %, female 38.9 %, mean age, 24.6±13.11 months, peak bilirubin levels...

MEHMET ALİ MALAS, ERKAN ATAŞ

2005, Vol 21, Issue 1, Page 5-10

Purpose: In this study, we aimed to determine the measurements and the relation between measured parameters of hand, second and fourth finger in full term, newborn with low birth weight and premature newborns. Materials and method: We were studied 60 premature newborns (Male 30, Female 30) who were...

ALİ ANNAGÜR, HÜSEYİN ALTUNHAN, SEBAHATTİN ERTUĞRUL, RAHMİ ÖRS

2009, Vol 25, Issue 4, Page 211-214

Oro-facio-digital syndrome, a group of congenital anomalies, is characterized by malformations of the oral cavity (cleft palate and tongue, abnormal dentition, high arched palate, tongue lobulation, hamartomata on the tongue), face (frontal bossing, facial asymmetry, hypertelorism, facial milia),...

ALİ ANNAGÜR, HÜSEYİN ALTUNHAN, HÜSEYİN TOKGÖZ, SABAHATTİN ERTUĞRUL, ÜMRAN ÇALIŞKAN, RAHMİ ÖRS

2011, Vol 27, Issue 1, Page 40-42

Congenital Leukemia is rare disease seen at birth or in the first 4 weeks of life . The incidence of Congenital Leukemia is 1 over 4.7 million live births. Most of the cases are myeloblastic leukemia. Usually symptoms like leukocytosis, petechia, echymosis, cutaneous nodules, hepatosplenomegaly and...

ŞADUMAN DİNÇER, MÜSLİM YURTÇU, ENGİN GÜNEL

2011, Vol 27, Issue 1, Page 46-51

To inform the doctors and nurses working in intensive care units about the pain in newborns, its effects on neonatal development, and the use of nonpharmacological methods for effective pain management. Newborns are challenged by several painful stimuli because of diagnostic and therapeutic...

ZEHRA KARATAŞ, MEHMET ARİF AKŞİT, NESLİHAN TEKİN

2011, Vol 27, Issue 2, Page 73-76

In recent years, increase in the frequency of positive direct Coomb’s (DC) test in newborns without blood incompatibilitiy is remarkable. The objective of the present study is to determine the associated factors that causing this increase. Ninety-seven patients with positive DC test from 2362...

ALİ ANNAGÜR, HÜSEYİN ALTUNHAN, RAHMİ ÖRS

2011, Vol 27, Issue 4, Page 255-259

Neonatal hemochromatosis is a rare disease clinically defined as severe neonatal liver disease in association with extrahepatic siderozis. The etiology of neonatal hemochromatosis is not understood exactly. However, according to a theory neonatal hemochromatosis is accepted to be an alloimmune...

ZEHRA KARATAŞ, TAMER BAYSAL, FATIH ŞAP, HAYRULLAH ALP, HAKAN ALTIN, SEVİM KARAASLAN

2012, Vol 28, Issue 3, Page 181-183

Absent pulmonary valve syndrome (APVS) is a rare congenital heart disease. It can be seen isolated or with other congenital heart diseases. Here, we presented a neonate with cyanosis and dyspnea because of APVS. A-female-newborn was referred to pediatric cardiology due to cyanosis, respiratory...

HAYRULLAH ALP, TAMER BAYSAL, ABDULLAH ALPINAR, SEVİM KARAARSLAN

2014, Vol 30, Issue Ek, Page 46-48

Anomalous left coronary artery from pulmonary artery (ALCAPA) is a rare congenital heart disease in which left coronary artery leaves from the pulmonary artery. Patients are usually asymptomatic in neonatal period during the pulmonary artery pressure decreases up to a critical level. However,...

ÖZKAN İLHAN, ESRA ARUN ÖZER, SÜMER SÜTÇÜOĞLU, SENEM ALKAN

2014, Vol 30, Issue 1, Page 8-11

Neonatal jaundice is usually a self-limiting benign clinical condition. International treatment guidelines to outline the borders of treatment of neonatal jaundice exist. The aim of our study is to evaluate the rationale of treatment guidelines for newborns admitted to the hospital for jaundice. In...

NİLÜFER GÜZOĞLU, BİRGÜL SAY, NURDAN URAS, UĞUR DİLMEN

2014, Vol 30, Issue 3, Page 137-138

Very long-chain fatty acid dehydrogenase (VLCAD) deficiency is an autosomal recessive disorder of mitochondrial fatty acid oxidation. Elevated plasma level of acyl-carnitine by Tandem mass spectrometry prompts the diagnosis of VLCAD. We herein report a neonate with a diagnosis of VLCAD whose...

MELİH YILDIZ, MEHMET ŞAH İPEK, FESİH AKTAR, BANU MUTLU ÖZYURT, REHA SERMED AYGÖREN

2015, Vol 31, Issue 1, Page 31-33

The diagnosis of a congenital diaphragmatic hernia (CDH) is often made on a prenatal ultrasound examination at routine obstetric care. After birth, the spectrum of respiratory symptoms in an infant with a CDH is determined by the degree of pulmonary hypoplasia. The most affected infants develop...

MİTHAT ARICIGİL, ALİ RIZA ULUTAŞ, ABİTTER YÜCEL, HAMDİ ARBAĞ

2015, Vol 31, Issue 3, Page 121-123

Hearing loss is one of the most commonly seen abnormalities in people. Hearing is essential for speech and cognitive functions during the first years of life and therefore early diagnosis and amplification is important. In our study we published the hearing screening results of newborns collected...

NURİYE EMİROĞLU, MURAT KONAK, TAMER ALTINOK, SEVGİ PEKCAN, KEMAL ÖDEV, RAHMİ ÖRS

2016, Vol 32, Issue Ek, Page 59-61

Congenital lobar emphysema (CLE) is a rare anomaly of lung development that presents in the neonatal period. A 13-day-old girl baby was admitted to our unit because of primary pulmonary hypoplasia. She had presented with severe dyspnea and cyanosis, where chest radiograph and chest computed...

NİLGÜN ALTUNTAŞ, HARUN PERU

2016, Vol 32, Issue 1, Page 25-27

Caesarean delivery is preferred to vaginal delivery in the breech presentation because it is safer. In this case report, we aimed to present femur fractures associated with cesarean section as a rare complication of breech presentation. A 2670g male infant was delivered at 36 weeks by emergency...

NURİYE EMİROĞLU, MURAT KONAK, HÜSEYİN ALTUNHAN, MÜSLİM YURTÇU, RAHMİ ÖRS

2017, Vol 33, Issue 4, Page 78-79

Congenital pyloric atresia (CPA) is an extremely rare condition. It may be isolated or accompanied by other abnormalities. In isolated cases, prognosis is good but congenital pyloric atresia can be fatal depending on another anomali. The etiology is still unknown. Since familial cases were reported...

SELMİN KARATAYLI ÖZGÜRSOY, ULAŞ ONAY, EMİNE POLAT, TÜLAY TOS

2017, Vol 33, Issue 4, Page 80-81

Facial asymmetry in new-born babies is not always due to facial paralysis. Congenital facial asymmetry, might as well as be due to depressor anguli oris muscle aplasia (DAOA), so called “congenital asymmetric crying facies”. Additional congenital anomalies like skeletal, cardiovascular, urogenital,...

SELVİ GÜLAŞI, ÜMİT ÇELİK

2018, Vol 34, Issue 1, Page 40-50

Invasive candidiasis is responsible for about 10% of nosocomial sepsis and it continues to be significant cause of serious morbidity and mortality in very low birth weight infants. Alhough the informations about the antifungal drugs which used for Candida species are increasing, studies and...