Articles on newborn

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...

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

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),...

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...

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...

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...

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,...