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   Keratosis follicularis spinulosa decalvans  
   
نویسنده qayoom s. ,sultan j. ,khan k.
منبع journal of pakistan association of dermatologists - 2016 - دوره : 26 - شماره : 3 - صفحه:260 -261
چکیده    A case of keratosis follicularis spinulosa decalvans in young kashmiri male is presented. this rare disorder with genetic and clinical heterogeneity,inherited in an x-linked recessive pattern is secondary to mutation in sat1 gene located at xp22.1. although multigenerational families with male to male transmission suggestive of autosomal dominant inheritance have been reported,we present a case with no family history.
کلیدواژه Keratosis follicularis spinulosa decalvans; Young male
آدرس department of dermatology,std and leprosy,skims medical college hospital, India, department of dermatology,std and leprosy,skims medical college hospital, India, postgraduate department of orthopedics,skims medical college hospital, India
 
     
   
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