نتایج جستجو برای: congenital varicella syndrome

تعداد نتایج: 728984  

Journal: :international journal of pediatrics 0
noor mohammad noori children and adolescent health research center, zahedan university of medical sciences and health services, zahedan, iran. alireza teimouri children and adolescent health research center, zahedan university of medical sciences and health services, zahedan, iran. maryam nakhaey moghaddam children and adolescent health research center, zahedan university of medical sciences and health services, zahedan, iran. touran shahraki children and adolescent health research center, zahedan university of medical sciences and health services, zahedan, iran.

background the prevalence of celiac disease (cd) is remarkably varied in down syndrome(ds)patientscompared with other diseases.  this study aimed to assess celiac disease prevalence in down syndrome children with and without congenital heart defects (chd) and its comparison with controls. materials and methods this case-control study was performed at a single center on 132 participants in three...

Journal: :گوارش 0
hassan saadatnia ali moatamedi

a fifteen-year-old torkaman girl with turner's mosaic kariotype is presented. she has had congenital esophageal stenosis with severe dysphagia since birth and iron deficincy anemia in addition to other classical features of the syndrome. according to author's knowledge this is the first report of a new congenital structural gastrointestinal anomaly with this disease.

Journal: :Pediatric Neurology Briefs 1993

2016
Tommy L. H. Chan Ana M. Cartagena Anne Marie Bombassaro Seyed M. Hosseini-Moghaddam

Ramsay Hunt syndrome associated with varicella zoster virus reactivation affecting the central nervous system is rare. We describe a 55-year-old diabetic female who presented with gait ataxia, right peripheral facial palsy, and painful vesicular lesions involving her right ear. Later, she developed dysmetria, fluctuating diplopia, and dysarthria. Varicella zoster virus was detected in the cereb...

Dear Editor-in-Chief: I read and enjoyed your stylish article, "Frequency of Congenital Cardiac Malformations in Neonates with Congenital Hypothyroidism", in relation to heart disease with hypothyroidism. As we know, one of the most commonly associated congenital hypothyroidism disorders is congenital heart disease, which has a significant effect on the recovery of pat...

2011
Fotinie Ntziora Athina Euthimiou Maria Tektonidou Anastasios Andreopoulos Kostas Konstantopoulos

INTRODUCTION We present a case of an unusual clinical manifestation of Guillain-Barre syndrome following a pre-existing herpes virus infection. Although there have been several reports describing the co-existence of herpes virus infection and Guillain-Barre syndrome, we undertook a more in-depth study of the cross-reactivity between herpes viruses and recommend a follow-up study based on serolo...

Journal: :Enfermedades infecciosas y microbiologia clinica 2010
Montserrat Muñoz-Sellart Carolina García-Vidal Sergio Martínez-Yelamos Jordi Niubó Pedro Fernández-Viladrich

BACKGROUND There is little information regarding peripheral facial palsy (PFP) as a complication of varicella. We describe 2 adults who developed varicella-related PFP, in 1 case as a part of Guillain-Barré syndrome (GBS), and review all reported cases of this condition. METHODS MEDLINE search. RESULTS A total of 10 cases of isolated varicella-associated PFP have been reported. PFP was diag...

Journal: :Archivos de la Sociedad Espanola de Oftalmologia 2006
J C López-García J Buesa-Gómez A Pardo-Saiz J Callizo-Tomás

CLINICAL CASE This was a 15-month-old boy who had macular retinochoroidal lesions in both eyes following maternal varicella during pregnancy. DISCUSSION The scars were suggestive of congenital chorioretinal infection, but because of negative serology and the clinical picture, we believe the problems are atypical macular colobomata.

Background: Oculo-palato-cerebral syndrome is an extremely rare condition characterized by various features, including low-birth weight, microcephaly, cerebral atrophy, mild-to-severe developmental delay, cleft palate, persistent hyperplastic primary vitreous, microphthalmia, small hands and feet, joint laxity, and large ears with thick helices. Diagnosis of this syndrome is based on the clinic...

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