نتایج جستجو برای: congenital sensory

تعداد نتایج: 211126  

Background and purpose: Sensory processing is necessary to perform daily activities properly. The aim of this study was to investigate the frequency of sensory processing disorder in children aged 5-11 years old. Materials and methods: This descriptive cross-sectional study included all children aged 5 to 11 years old in kindergartens and primary schools in Tehran, Iran. Children meeting the i...

2012
Mehmet Erdil Kerem Bilsel Yunus Imren Hasan Huseyin Ceylan Ibrahim Tuncay

INTRODUCTION Congenital insensitivity to pain, a rare neurological entity, is characterized by varying degrees of sensory loss and autonomic dysfunction. Orthopedic manifestations of congenital insensitivity to pain include delayed diagnosis of fractures, nonunions, malunions, Charcot arthropathy, acro-osteolysis, avascular necrosis, osteomyelitis, heterotopic ossification and joint dislocation...

Journal: :Turk pediatri arsivi 2014
Ahmet Kağan Özkaya Ekrem Güler Elif Arık Ali Rıza Namlı Derya Cevizli Olcay Güngör

Congenital insensitivity to pain with anhidrosis (CIPA) syndrome is a rare autosomal recessive disease which is also known as hereditary sensory and autonomic neuropathy type 4 (1). The prominent characteristics of the disease include fever due to anhidrosis, absence of sense of pain, painless ulcers in the structures inside the mouth and extremities, self-harm behavior, mild to severe mental r...

2008
Lisa Putzar Ines Goerendt Kathrin Lange Frank Rösler Brigitte Röder

Animal studies have shown that visual deprivation during the first months of life permanently impairs the interactions between sensory systems. Here we report an analogous effect for humans who had been deprived of pattern vision for at least the first five months of their life as a result of congenital binocular cataracts. These patients showed reduced audiovisual interactions in later life, a...

2012
Prateek Gehlot Jagdish Mandliya

Caudal regression syndrome (CRS) is a rare neural tube defect affecting terminal spinal segments and cord manifesting as neurological deficit ranging from bladder and bowel involvement to severe sensory motor deficits in lower limbs. It has sporadic appearance and maternal diabetes, genetic factors, teratogens and hypoperfusion are considered as possible etiologic factors and it can be associat...

Journal: :Neurology 2010
C A Lyle D Malicki M O Senac M L Levy J R Crawford

A full-term infant with an uncomplicated vaginal delivery presented with absent cry on routine newborn heelstick testing. Neurologic examination revealed paraplegia, absent reflexes, and a T4 sensory level. Spinal MRI showed an expansive, gadolinium-enhancing intramedullary mass from T2 to the thecal sac (figure, A and B). Biopsy confirmed a diagnosis of cellular schwannoma, WHO grade 1 (figure...

Journal: :Pediatric dentistry 2016

Special health care needs include any physical, developmental, mental, sensory, behavioral, cognitive, or emotional impairment or limiting condition that requires medical management, health care intervention, and/or use of specialized services or programs. The condition may be congenital, developmental, or acquired through disease, trauma, or environmental cause and may impose limitations in pe...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1998

2014
Hristo Georgiev Georgi P Georgiev

The treatment of severe rigid neurogenic clubfoot deformities still remains a challenging problem in modern paediatric orthopaedics. In those cases, in spite of being a palliative procedure, talectomy has been advocated for the correction of the deformity thus providing a stable plantigrade foot which allows pain-free walking with standard footwear. Herein, we present the results after talectom...

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