نتایج جستجو برای: congenital varicella syndrome

تعداد نتایج: 728984  

Journal: :iranian red crescent medical journal 0
a matic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected]; neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] s pricic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] m matic clinical centre of vojvodina, dermatovenereological clinic, serbia g velisavljev filipovic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] a ristivojevic neonatology department, gynaecologic-obstetric clinic, clinical centre of vojvodina, serbia

background cutis marmorata telangiectatica congenita (cmtc) is a sporadic congenital skin vascular abnormality. significant number of patients has other congenital anomalies. case report we report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. besides, microretrognatia and asymm...

2014
Eva Rye Rasmussen Eva Lykke Jan Gren Kristianna Mey

Introduction: The Ramsay Hunt syndrome is characterized by herpetic lesions combined with peripheral facial nerve palsy. The disease is caused by a reactivation of the varicella zoster virus and can be deceiving since the herpetic lesions are not always present (zoster sine herpete) and might mimic other severe neurological illnesses. This article reviews the various forms of Ramsay Hunt syndro...

2013
Lucy Pembrey Pauline Raynor Paul Griffiths Shelley Chaytor John Wright Andrew J. Hall

OBJECTIVE To estimate the seroprevalence of cytomegalovirus (CMV), Epstein Barr virus (EBV) and varicella zoster virus (VZV) among pregnant women in Bradford by ethnic group and country of birth. METHODS A stratified random sample of 949 pregnant women enrolled in the Born in Bradford birth cohort was selected to ensure sufficient numbers of White UK born women, Asian UK born women and Asian ...

2013
Yil Ryun Jo Chin Wook Chung Jung Soo Lee Hye Jeong Park

Vernet syndrome involves the IX, X, and XI cranial nerves and is most often attributable to malignancy, aneurysm or skull base fracture. Although there have been several reports on Vernet's syndrome caused by fracture and inflammation, cases related to varicella-zoster virus are rare and have not yet been reported in South Korea. A 32-year-old man, who complained of left ear pain, hoarse voice ...

Journal: :Brain & Development 2021

Background Microcephalic osteodysplastic primordial dwarfism type I (MOPD I, also known as Taybi-Linder syndrome) is a rare genetic disorder associated with severe intrauterine growth retardation, short stature, microcephaly, brain anomalies, stunted limbs, and early mortality. RNU4ATAC, the gene responsible for this disorder, does not encode protein but instead U4atac small nuclear RNA (snRNA)...

2014
Byung Ok Kwak Min Jung Lee Hye Won Park Min Kyung Song Sochung Chung Kyo Sun Kim

Varicella is usually considered to be a benign disease in healthy children; however, serious complications can occur such as necrotizing fasciitis and toxic shock syndrome. We describe a 38-month-old girl with necrotizing fasciitis and streptococcal toxic shock syndrome following varicella. She was previously healthy and vaccinated against varicella at 12 months of age. She had been diagnosed w...

Journal: :Pediatric Research 2001

2015
Takashi Shinha Pasala Krishna

Ramsay Hunt syndrome is characterized by varicella zoster virus infection affecting the geniculate ganglion of the facial nerve. It typically presents with vesicles in the external auditory canal associated with auricular pain and peripheral facial nerve paralysis. Although vestibulocochlear nerve is frequently co-involved during the course of Ramsay Hunt syndrome, multiple lower cranial nerve ...

Journal: :acta medica iranica 0
z moinfar f. davari tanha z. moinfar m. kaveh s. eftekhari s. eftekhari z. khalilpour

short rib polydactyly syndrome (srps) is a very rare congenital anomaly that is classified into four subtypes. it is an autosomal recessive inherited disease. we report a case of this syndrome without a previous family history of congenital defects.

2017
Lucy Pembrey Pauline Raynor Paul Griffiths Shelley Chaytor John Wright Andrew J. Hall

Objective: To estimate the seroprevalence of cytomegalovirus (CMV), Epstein Barr virus (EBV) and varicella zoster virus (VZV) among pregnant women in Bradford by ethnic group and country of birth. Methods: A stratified random sample of 949 pregnant women enrolled in the Born in Bradford birth cohort was selected to ensure sufficient numbers of White UK born women, Asian UK born women and Asian ...

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