نتایج جستجو برای: infant jaundice

تعداد نتایج: 101022  

2014
Marco Pezzati

Neonatologists generally recognize that late preterm infants face more problems in the immediate newborn period compared with their full-term counterparts. [1,2]. This excess morbidity extends beyond the initial birth hospitalization [3] and the literature recognizes that readmission rates of late preterm infants are 1.5 to 3 times that of term infants [4-7]. In this group of infants, the overw...

2014
Nurcan Özyazıcıoğlu Sevinç Polat

The aim of this study is to identify some traditional practices used for the newborn babies in Turkey and to discuss the possible effects of these practices upon the health of the babies. The traditional care practices (salting, swaddling, holluk, starting breastfeeding late, practices against newborn jaundice, making the forties, etc.) reported to be most prevalent between January 2008 and Oct...

Journal: :Pediatrics 2000
T W Hansen

Neonatal jaundice must have been noticed by caregivers through the centuries, but the scientific description and study of this phenomenon seem to have started in the last half of the 18th century. In 1785 Jean Baptiste Thimotée Baumes was awarded a prize from the University of Paris for his work describing the clinical course in 10 jaundiced infants. The work by Jaques Hervieux, which he defend...

Journal: :Journal of Hematology & Oncology 2009
Hideki Yoshida Hiroyuki Ishida Takao Yoshihara Takashi Oyamada Masataka Kuwana Toshihiko Imamura Akira Morimoto

Hereditary spherocytosis (HS) is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice and splenomegaly. Evans' syndrome is a clinical syndrome characterized by autoimmune hemolytic anemia (AIHA) accompanied by immune thrombocytopenic purpura (ITP). It results from a malfunction of the immune system that produces multiple autoantibodies targeting at leas...

Journal: :Einstein 2011
Taísa Roberta Ramos Nantes de Castilho Marcelli Salete Vargas Adriana Pinsuti Marcos Augusto Rocha Jose Ricardo D'Bertagnon

The authors present the case of a newborn of an Rh-factorsensitized mother, who received early hospital discharge while icteric only to be readmitted at an Emergency Service at five days of age with signs of kernicterus. Despite treatment given, the neonate progressed with a clinical picture of bilirubin encephalopathy. The lack of interaction between the obstetric and neonatal teams, premature...

Journal: :The Medical journal of Australia 2017
Lachlan J Warren Dev Tilakaratne Rakesh Seth

Clinical images Day 5: widespread indurated truncal plaques due to Trichophyton rubrum superficial dermatophyte infection (A and B) Following chorioamnionitis, a male infant from a remote Indigenous community was born by vaginal breech delivery at 26 weeks’ gestation. On Day 5, indurated, vesicular and erythematous lesions were noted on extensive areas of the back (Box, A and B). Blue light (45...

Journal: :The Yale Journal of Biology and Medicine 1959
Margaret J. Albrink

rubin is discussed along with the disorders, particularly jaundice and the consequences thereof, which occur in a premature infant and in members of a certain strain of rats, because both the latter groups cannot effectively conjugate bilirubin to its excretable form. A therapeutic program designed to overcome the enzymatic defect in jaundiced human infants is reviewed; unfortunately, work done...

2017
Noella Maria Delia Pereira Ira Shah

Cholestasis can occur in newborns due to infections. However, the manifestations of the underlying infections usually dominate the presentation. We present a 2-month-old infant who presented with jaundice and no fever or signs of systemic illness. Liver biopsy was suggestive of cholangitis. He was subsequently detected to have urinary tract infection with Klebsiella pneumoniae. The child was tr...

2011
Ahmad Khodadad Vajiheh Modaresi Mohammad-Ali Kiani Ali Rabani Bahar Pakseresht

BACKGROUND Lipoid congenital adrenal hyperplasia, is the rarest and usually the most severe form of adrenal steroidogenic defect,which may presents as infantile cholestasis. CASE PRESENTATION Here we present a 45 days old infant who came to our attention with cholestasis and severe intractable vomiting and electrolyte disturbances. Evaluation resulted in diagnosis of congenital adrenal hyperp...

2014
Tamer Rizk Adel Mahmoud Tahani Jamali Salah Al-Mubarak

Aim. We aim to describe a female patient with Menkes disease who presented with epilepsia partialis continua. Case Presentation. Seventeen-months-old Saudi infant was presented with repetitive seizures and was diagnosed to have epilepsia partialis continua. Discussion. Menkes disease (OMIM: 309400) is considered a rare, X-linked recessive neurodegenerative disorder resulting from a mutation in ...

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