Leopard syndrome
A genetic syndrome caused by mutations in the PTPN11 and RAF1 genes. It is characterized by the following abnormalities: multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities in genitalia, growth retardation, and deafness.
Disease Alternative Name
Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )
Regional Research Institute of Unani Medicine
Research Associate
NATIONAL INSTITUTE OF UNANI MEDICINE
MD Moalijat (Medicine)
Attached 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.
BCCL Hospital
Ex. Dy.Cmo
PMCH
MBBS
Consultancy
MBBS DHL
IGICH
Registrar
MSRMC
MBBS
Vijaya Hospital
Pg Student