A profile of childhood neuropathies at a University Hospital in Oman

Roshan Koul*, Alexander Chacko, Hashim Javed, Khalid Al-Hinai, Matthew Zachariah, Srinivas Bulusu, Thirapathur V. Rao

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةArticleمراجعة النظراء

15 الاقتباسات (SciVal)


Objective: To analyze all cases of child childhood neuropathies (under 14 years of age) and report on their profile, pattern, clinical features and management. Methods: Children with acute flaccid paralysis, longstanding weakness of extremities, neuroregression and children receiving anti cancer drugs with symptoms suggestive of neuropathy were evaluated for evidence of peripheral neuropathy. The evaluation of children with acute flaccid paralysis was a prospective study from January 1992 through to December 2000. The rest of the patients were studied retrospectively from the hospital medical records, pediatric neurology outpatient clinic and the neurophysiology laboratory, Sultan Qaboos University Hospital, Al-Khod, Oman. Results: Eighty-two (39 Male: 43 Female) children were found to have peripheral neuropathy. Acute Guillian-Barre syndrome was the most common with 37 children (45.1%), followed by genetic neuropathies [hereditary motor and sensory neuropathy with 17 (20.7%), hereditary sensory and autonomic neuropathy with 2 (2.4%), hereditary spastic paraplegia associated neuropathy with 9 (11%) and metachromatic leucodystrophy with 9 (11%)]. Chronic inflammatory demyelinating neuropathy was seen in 5 (6.1%) and vincristine induced neuropathy in 3 (3.5%) children. Conclusion: Acute Guillian-Bare syndrome is the most common neuropathy amongst the acquired neuropathies. The treatable neuropathies constituted 54.7% (45 children) and the preventable genetic neuropathies accounted for the remaining 45.3% (37 children).

اللغة الأصليةEnglish
الصفحات (من إلى)450-456
عدد الصفحات7
دوريةSaudi Medical Journal
مستوى الصوت23
رقم الإصدار4
حالة النشرPublished - 2002

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