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dc.contributor.authorBahemuka, M
dc.contributor.authorBrown, JD
dc.date.accessioned2013-06-11T08:48:31Z
dc.date.available2013-06-11T08:48:31Z
dc.date.issued1982-08
dc.identifier.citationDev Med Child Neurol. 1982 Aug;24(4):519-24en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/7117711
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31313
dc.description.abstractFive children, three sisters and two brothers aged between three months and 12 years, are described. They all developed a facial desquamating rash of butterfly distribution at the age of about two months, and motor retardation which later was characterized by spasticity, predominantly affecting the lower limbs. The three children who were old enough for speech to be tested had dysarthria. There was no family history of neurological disease, nor was there consanguinity among the parents or grandparents. EEGs were diffusely abnormal in four of the five children, but did not show any specific or diagnostic features. Plasma immunoglobulin tests were normal, and tests for collagen disease were negative. The authors are not aware of previous reports of this condition, but believe that it is a variant of familial spastic paraplegia, with atypical features.en
dc.language.isoenen
dc.publisherUnivesity of Nairobien
dc.titleHeredofamilial syndrome of spastic paraplegia, dysarthria and cutaneous lesions in ive siblings.en
dc.typeArticleen
local.publisherDepartment of Medicineen


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