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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HOLISTIC HEALTH CONSULTANT PRACTISING COMPLEMENTARY& INTEGERATED MEDICINE Especially EBH..Evidence Based HOMOEOPATHY Since 1984 *****************************************************A Ph.D Thesis Guide & Assessor
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MKCG MCH
MBBS and MD (pediatrics)

Aarogyadham Clinic
Consulting Physician
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Gauhati Medical College and Hospital
Retd. Professor of Pediatrics. Gauhati Medical College. Assam. Presently Guest Faculty, Dnb Pediatrics. Apollo Hospital. Guwahati. Assam
Assam Medical College & Hospital,Dibrugarh
MD (Pediatrics)

