نتایج جستجو برای: facial diplegia

تعداد نتایج: 60920  

Journal: :The British journal of ophthalmology 1957
H REED W GRANT

Various terms have been applied to this condition: Mobius's syndrome, congenital facial diplegia, congenital oculo-facial paralysis, nuclear agenesis, and congenital nuclear aplasia. It was originally described by von Graefe (1880), Harlan (1881), and Chisolm (1882). M6bius (1892) collected 43 cases of congenital and acquired cranial nerve palsies and classified them into six groups. One group ...

Journal: :JAMA: The Journal of the American Medical Association 1905

Journal: :Archives of Disease in Childhood 1991

Journal: :Bulletin of Faculty of Physical Therapy 2023

Abstract Background Children with spastic diplegia experience gait abnormalities and problems caused by deficits in balance, motor control, spasticity. Abnormal pelvic inclination is common patients which may result poor balance. Purpose This study was conducted to investigate the relation between standing balance children diplegia. Subjects methods Thirty diplegic cerebral palsy from both sexe...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2016

Journal: :Neuroscience and Medicine 2022

Introduction: Sjögren’s syndrome is an autoimmune epithelitis with various extraglandular signs, among which are neurological, a variable frequency according to studies. We report three cases of peripheral neuropathy revealing Gougerot-Sjögren’s syndrome, collected in the Neurology Department Fann University Hospital Dakar (Senegal). Observations: The first patient, aged 48 years, presented len...

Journal: :American journal of medical genetics. Part A 2006
Anna Rajab Seung-Yun Yoo Aiman Abdulgalil Salem Kathiri Riaz Ahmed Ganeshwaran H Mochida Adria Bodell A James Barkovich Christopher A Walsh

Cerebral palsy (CP) is defined as any nonprogressive motor deficits resulting from cerebral abnormalities that occur in the prenatal or perinatal period. Symptoms become apparent during the first year of life. Genetic forms of CP account for about 2% in European populations but are thought to cause a substantial proportion in consanguineous families. We have identified a large consanguineous fa...

Journal: :Acta Radiologica 1996

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