نتایج جستجو برای: omphalitis

تعداد نتایج: 134  

Journal: :Archives of disease in childhood 1977
M Odièvre G Pigé D Alagille

Congenital abnormalities were present in 12 out of 30 (40%) children with extrahepatic portal hypertension of unknown cause, but in only 2 out of 17 (12%) children with extnahepatic portal hypertension secondary to umbilical vein catheterization or omphalitis. The most frequent abnormalities in this series and in published reports were atrial septal defect, malformation of the biliary tract, an...

Journal: :Asian Community Health Nursing Research 2022

One of the traditional methods for umbilical cord care in Indonesia is campuh method, which uses turmeric and betel leaves. The purpose this research to find out how mothers Traditional Birth Attendants (TBAs) perform newborns using method Sukawana Village, Curug District, Serang City, Banten Province. This a descriptive qualitative with case study design. Interviews were conducted who used tak...

Journal: :Medical archives 2012
Ugur Kesici Asiye Yenisolak Sevgi Kesici Cigdem Siviloglu

INTRODUCTION Primary umbilical endometriosis a rare case. It is mostly seen in women in the reproductive age group. CASE REPORT In this case report, a 38 year old woman is discussed who received antibiotherapy for omphalitis diagnosis established due to many complaints of umbilical secretion but who was diagnosed with primary umbilical endometriosis after histopathological examination. CONC...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2013
Mohammad Golshan Nematizadeh Hossein

OBJECTIVE To compare the extraction time and infection rate of umbilical cord by applying ethanol, humanmilk or dry care. METHOD The parallel single-blinded randomised clinical trial was performed on 300 neonates at Shahid Sadougi University of Medical Sciences and Health Service, Yazd, Iran, between March and September 2010. The neonates were divided into three random but numerically equal g...

Journal: :Acta medica Iranica 2010
Zohreh Kavehmanesh Zahra Khalili Matinzadeh Susan Amirsalari Mohammad Torkaman Shahla Afsharpayman Morteza Javadipour

Leukocyte adhesion deficiency type 1 (LAD 1) is an autosomal recessive hereditary disorder resulting from deficiency of CD18, characterized by recurrent bacterial infections. We report two consanguineous patients with Leukocyte adhesion deficiency type 1( LAD1). These two infant boy patients were referred to us, within a short period of time, with the complaints of recurrent infections at the a...

Journal: :International Journal of TROPICAL DISEASE & Health 2014

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