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Lamellar Ichthyosis with Rickets
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نویسنده
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Ali Raafia ,Aman Shahbaz ,Nadeem Muhammad
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منبع
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pakistan journal of medical sciences - 2013 - دوره : 29 - شماره : 2 - صفحه:660 -662
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چکیده
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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.
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کلیدواژه
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Lamellar ichthyosis ,Rickets ,Vitamin D deficiency.
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آدرس
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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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Authors
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