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   Neurofibromatosis type 1: Persisting misidentification of the elephant man disease  
   
نویسنده legendre c.-m. ,charpentier-côté c. ,drouin r. ,bouffard c.
منبع journal of the american board of family medicine - 2011 - دوره : 24 - شماره : 1 - صفحه:112 -114
چکیده    Background: during informal interviews in the course of an ethnographic study on intergenerational dialogue between individuals with neurofibromatosis and their parents,many members of canadian neurofibromatosis associations have stated that they continue to be told the condition that afflicts them or their children is elephant man's disease. today,even though well-established clinical criteria make it possible to diagnose and differentiate the 2 diseases,the confusion between neurofibromatosis type 1 (nf1) and elephant man's disease persists in both the media's and physicians' representations. methods: this was an ethnographic study in medical anthropology. discussion: some reference sources and print and online news media have all contributed to the persistence of the association between nf1 and elephant man's disease. our observations suggest that confusing nf1 with the elephant man's condition harms the interests of those with nf1 and thus increases the burden of the disease. conclusion: changes of attitude regarding medical teaching and the media could dispel the confusion among physicians and journalists.
کلیدواژه Elephant man; Genetic disease; Neurofibromatosis; Proteus syndrome; Psychosocial impact
آدرس division of genetics,department of pediatrics,université de sherbrooke,sherbrooke,qc j1h 5n4, Canada, division of genetics,department of pediatrics,université de sherbrooke,sherbrooke,qc j1h 5n4, Canada, division of genetics,department of pediatrics,université de sherbrooke,sherbrooke,qc j1h 5n4, Canada, division of genetics,department of pediatrics,université de sherbrooke,sherbrooke,qc j1h 5n4, Canada
 
     
   
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