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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Top doctors who continously share their opinions on Congenital ichthyosisAttached To Charitable Organizations As Honorary Holistic Health Consultant
HOLISTIC HEALTH CONSULTANT PRACTISING COMPLEMENTARY& INTEGERATED MEDICINE Especially EBH..Evidence Based HOMOEOPATHY Since 1984 *****************************************************A Ph.D Thesis Guide & Assessor
M.D..FF.HOM, D.A.c..D.Sc.

Self Employed. Now Doing My Practice
Pediatric Consultant
MKCG MCH
MBBS and MD (pediatrics)

Aarogyadham Clinic
Consulting Physician
DISHA HOMEOPATHIC MEDICAL COLLEGE
BHMS

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)


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Tibial aplasia and prosthetic Leg restoration. *Chief Complaints* Due to congenital anomalies she walks with abnormal gait patterns. *History* When she was born 28 years ago with such congenital anomalies. Her parents never thought that their 5th girl child would be the same as others 4 . But she had different problems with tibial aplasia and others 4 having complex syndactyly in both hands. Same as their father having complex syndactyly. *Vitals* Unable to perform activities of daily living. *Physical Examination* Problem with walking and gripping and grasping. *Management* 28 years old girl looking for Prosthetics management for tibial aplasia. Our team takes measurements and casting for Prosthetic Leg restoration. Now she walks comfortably with a new prosthetic Leg.
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