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
Trending Cases
What is the treatment of ulcer in angle of both lips again and again? I give tess oint there is recover but it produce again what is cause and treatment?
Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer