نتایج جستجو برای: organ disorder syndrome

تعداد نتایج: 1220503  

Journal: :archives of pediatric infectious diseases 0
atmaram pawar department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india asawari raut department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india; department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india. tel: +91-9960821040 vijay kalrao pediatrics department, bharati vidyapeeth university, bharati hospital, pune, india john jacob department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india isha godha department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india ritty thomas department of clinical pharmacy, poona college of pharmacy, bharati vidyapeeth university, pune, india

background sepsis can be defined as the body’s response to an infection. sepsis in children remains a significant cause of morbidity and mortality worldwide. objectives this study focuses on the etiological factors, risk factors, and clinical characteristics of sepsis in neonate and pediatric patients. patients and methods a prospective study was conducted over a six-month period in the pediatr...

Journal: :Indian pediatrics 2004
Ramazan Kutlu Alpay Alkan Onur Kutlu Cengiz Yakinci

Seckel syndrome is a rare genetic disorder with a typical "bird-headed" appearance. It could affect many organ systems but renal involvement is uncommon. Polyarteritis nodosa is systemic vasculitic disorder which also involves kidneys. We report a case of Seckel syndrome in a 9 year-old boy with renal involvement due to polyarteritis nodosa. According to the literature, this is the first report...

Journal: :Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2011
Xiang-Rong Zheng Fei Yin Rong Huang Qiu-Lian Xiang

The Bardet-Biedl syndrome (BBS) is a rare ciliopathic human autosomal-recessive disorder, affecting multiple organ systems. Kidney abnormalities are a major cause of morbidity and mortality in Bardet-Biedl syndrome.

Journal: :acta medica iranica 0
mehri najafi sani department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. mitra ahmadi research center for immunodeficiencies, children's medical center, tehran university of medical sciences, tehran, iran. pejman roohani department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. nima rezaei research center for immunodeficiencies, children's medical center, tehran university of medical sciences, tehran, iran. َand department of immunology, school of medicine, tehran university of medical sciences, tehran, iran. and 4universal scientific education and research network (usern), tehran, iran.

zellweger syndrome (zs) is a peroxisomal disorder with a multiple congenital anomalies, characterized by stereotypical facies, profound hypotonia, organ involvement including cerebral, retinal, hepatic, and renal. herein, a 3-month-old female with zs is presented who was referred because of increased liver enzymes (subclinical hepatitis), which was detected in work-up of her neck cyst, severe h...

Journal: :Medical journal of Zambia 2022

Abstract
 Hunter syndrome is one of the Mucopolysaccharidosis (MPS), type II. It a rare genetic disorder due to deficiency in enzyme Iduronate 2-sulphatase. This leads accumulation glycosaminoglycans (GAGs) dermatan sulphate and heparan sulphate. The GAGs accumulate both intracellularly extracellularly, leading abnormalities different organ systems body. definitive diagnosis requires bioch...

Journal: :Journal of family medicine 2022

Polycystic Ovarian Syndrome (PCOS) is endocrine and gynecological disorder that affects women of reproductive age. This a case report patient with PCOS who was misdiagnosed presented several symptoms. emphasizes the need for holistic healthcare approach to treat underlying organ dysfunction in PCOS. It highlights interconnectedness between dysfunction. examines chronic inflammatory state, risk ...

Journal: :Sestrinski glasnik 2021

Down syndrome [DS] is the most common chromosomal disorder in population manifested by intellectual disabilities of varying degrees, often accompanied disorders organ systems. Compared to children without DS, these have a greater risk developing malignancy such as acute leukemia. Leukemia blood cells and lymph nodes form cancer children. Its treatment with DS more complex compared this syndrome...

Journal: :مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 0
ملیحه کدیور m kadivar سعیده سلمان زاده s salmanzadeh

sepsis is the systemic response to severe infection in critically ill patients. sepsis, septic syndrome & septic shock represent the increasingly severe stages of the same disease. despite the remarkable improvements in outcome, sepsis & septic shock remain an important cause of morbidity & mortality in children. this is a retrospective study among the patients who were admitted in the pediatri...

Journal: :Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2015
Ricardo Duarte Humberto Morais

Polysplenia/heterotaxy syndrome is a rare congenital disorder associated with a wide spectrum of anomalies in various organ systems. Although anomalies of the cardiovascular system are common in this syndrome, the authors report a rare case of polysplenia syndrome associated with aortic pseudocoarctation, which to our knowledge has never been reported.

Journal: :acta medica iranica 0
mehri najafi sani department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. mitra ahmadi department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. pejman roohani department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. nima rezaei research center for immunodeficiencies, children's medical center, tehran university of medical sciences, tehran, iran. and department of immunology, molecular immunology research center, school of medicine, tehran university of medical sciences, tehran, iran. and network of immunity in infection, malignancy and autoimmunity (nima), universal scientific education and research network (usern), tehran, iran.

zellweger syndrome (zs) is a peroxisomal disorder with a multiple congenital anomalies, characterized by stereotypical facies, profound hypotonia, organ involvement including cerebral, retinal, hepatic, and renal. herein, a 3-month-old female with zs is presented who was referred because of increased liver enzymes (subclinical hepatitis), which was detected in work-up of her neck cyst, severe h...

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