Autosomal recessive congenital ichthyosis
An autosomal recessive condition caused by mutation(s) in the ALOX12B gene, encoding arachidonate 12-lipoxygenase, 12R-type. It is characterized by dry, thickened, scaly skin.
Disease Alternative Name
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Sir T. General Hospital
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MKCG MCH
MBBS and MD (pediatrics)
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