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   Lamellar Ichthyosis with Rickets  
   
نویسنده Ali Raafia ,Aman Shahbaz ,Nadeem Muhammad
منبع pakistan journal of medical sciences - 2013 - دوره : 29 - شماره : 2 - صفحه:660 -662
چکیده    Lamellar ichthyosis (li) is a rare genetic disorder with autosomal recessive inheritance. it is equally seen in both sexes and usually manifests at birth. the child presents as a collodion baby. the erythema is minimal or absent; but when present, it is maximum on the face. the scaling is generalized, accentuated on lower extremities and flexural areas. rickets is a condition in which there is softening of bones leading to fractures and deformities. it is caused by vitamin d deficiency & lack of adequate calcium in diet. children, 6 to 24 months of age, are at a higher risk due to rapidly growing bones. the association between various types of ichthyoses and rickets is well documented. we report a case of lamellar ichthyosis with rickets in a 14-year-old girl from our part of the world.
کلیدواژه Lamellar ichthyosis ,Rickets ,Vitamin D deficiency.
آدرس King Edward Medical University, Mayo Hospital, Department of Dermatology, Pakistan, King Edward Medical University, Mayo Hospital, Department of Dermatology, Pakistan, King Edward Medical College, Mayo Hospital, Department of Dermatology, Pakistan
 
     
   
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