Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Benign Congenital Hypotonia"'
Autor:
P. M. T. Dawson, T. Puckree
Publikováno v:
South African Journal of Physiotherapy, Vol 62, Iss 1, Pp 2-6 (2006)
Benign Congenital Hypotonia (BCH) is a condition whose specific diagnosis and causes are elusive. Time and intensive diagnostic screening allows for unmasking of a specific diagnosis in some cases. The remaining cases are considered to have a good pr
Externí odkaz:
https://doaj.org/article/c3a40466dfe645c4aa89af45bdeefa13
Autor:
J Gordon Millichap
Publikováno v:
Pediatric Neurology Briefs, Vol 12, Iss 9, Pp 69-70 (1998)
Twenty five children diagnosed with benign congenital hypotonia (BCH) between infancy and 2 years of age were examined at 6 to 8 years of age and compared to 26 controls, matched for sex, age, and weight, in a study at the School of Occupational Ther
Externí odkaz:
https://doaj.org/article/f110e5a2e6d84d82977291b5f95ce4a5
Autor:
John N. Walton
Publikováno v:
Developmental Medicine & Child Neurology. 2:10-18
The traditional concepts of hypotonic disorders in infancy need to be revised. These disorders are well grouped under: (1) infantile spinal muscular atrophy; (2) symptomatic hypotonia; and (3) benign congenital hypotonia. The clinical picture of the
Publikováno v:
Pediatric Neurology. 26:383-386
Congenital hypotonia with favorable outcome is characterized by an early neonatal onset and a benign clinical course. The old term, proposed by Walton, was benign congenital hypotonia, denoting the presence of muscle weakness and hypotonia, with the
Autor:
Suraj Gupte
Publikováno v:
Instructive Case Studies in Pediatrics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a3f110025df9bcd8f8826f812dbe8d6
https://doi.org/10.5005/jp/books/11434_13
https://doi.org/10.5005/jp/books/11434_13
Autor:
Peter B. Kang
Publikováno v:
The Clinical Neurophysiology Primer ISBN: 9780896039964
A variety of neuromuscular conditions affect children, ranging from severe, usually fatal disorders, such as spinal muscular atrophy type I (Werdnig-Hoffman syndrome) to relatively mild problems, such as benign congenital hypotonia. The evaluation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59d75074469153ef5eba5d5382014f23
https://doi.org/10.1007/978-1-59745-271-7_22
https://doi.org/10.1007/978-1-59745-271-7_22
Publikováno v:
Journal of child neurology. 18(3)
The records of all patients attending a neurosensory genetics clinic over an 11-year period were reviewed. Of the 450 patients seen, 31 presented with sensorineural hearing loss, hypotonia, and delay in the acquisition of motor milestones. Of these,
Autor:
Jms Pearce
Publikováno v:
Journal of Neurology, 251(8), 1028-1029. SPRINGER HEIDELBERG
Oppenheim’s name is perpetuated by his eponymous sign of pyramidal tract lesions, and by the disease bearing his name, Oppenheim’s disease. Amyotonia congenita1 is a congenital, sometimes familial, disorder, characterised by muscular hypotonia an
Autor:
V. K. Rehan, M. M. K. Seshia
Publikováno v:
Archives of Disease in Childhood. 69:92-94
Improvements in obstetric care have certainly led to a decrease in the incidence of birth related spinal cord trauma but unfortunately it is still encountered from time to time. Its exact incidence is difficult to determine because the spinal cord is
Autor:
Bar‐Efrat, Shula Parush, Asher Ornoy, Idit Yehezkehel, Alex Tenenbaum, Esther Tekuzener, Adam S. Jessel, Idit Hirsch
Publikováno v:
Developmental medicine and child neurology. 40(7)
In order to clarify the prognosis of benign congenital hypotonia (BCH), 25 children aged 6 to 8 years who had been diagnosed with BCH as infants were examined on a variety of sensory, perceptual-motor, and behavioural measures and compared with 26 co