Muscle weakness in children with neurofibromatosis type 1
نویسندگان
چکیده
منابع مشابه
Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
BACKGROUND Neurofibromatosis type 1 (NF1) is related to a generally increased prevalence of seizures. The mechanism underlying the increased predisposition to seizures has not been fully elucidated. The aim of the study was to evaluate the role of NF1 in seizures pathogenesis in a cohort of children with NF1 and seizures. METHODS The medical records of 437 children (0-18 years old) with NF1 w...
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Children with neurofibromatosis type 1 (NF1) are predisposed to malignancies such as brain tumors, leukemia, and pheochromocytomas. The aim of this study was to evaluate malignancy in patients with NF1. We studied 120 patients with NF1 in this study. Demographic data from these patients were retrospectively reviewed. We found 20 malignancies in 19 patients in our study. Ten children with NF1 ha...
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چکیده ندارد.
15 صفحه اولVitamin D status and muscle function in children with neurofibromatosis type 1 (NF1).
OBJECTIVES The aim of this cross-sectional study was to assess the vitamin D status and muscle function in children with NF1 compared with their unaffected siblings. METHODS NF1 children between 5 and 18 years of age and who had at least one unaffected sibling were identified. Serum concentrations of 25-hydroxyvitamin D (25(OH)D), calcium, inorganic phosphate, alkaline phosphate, parathyroid ...
متن کاملNeurological comorbidity in children with neurofibromatosis type 1.
BACKGROUND The aim of this study was to determine the frequency of central nervous system comorbidities in children with neurofibromatosis type 1 (NF1). METHODS We performed a nationwide survey to investigate neurological comorbidities in 3-15-year-old children with NF1 in Japan by sending questionnaires to pediatricians and pediatric neurologists. A secondary questionnaire was sent to the pa...
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ژورنال
عنوان ژورنال: Developmental Medicine & Child Neurology
سال: 2015
ISSN: 0012-1622
DOI: 10.1111/dmcn.12777