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
multiple lentigines syndrome
lentigines
electrocardiographic conduction defects
0cular hypertelorism
pulmonary stenosis
abnormalities of the genitals
retarded growth
deafness
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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
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