Noonan syndrome
A genetic syndrome caused by mutations in the PTPN11 gene (over 50% of the cases) or less frequently mutations in the SOS1, RAF1, or KRAS genes. It is characterized by short stature, webbed neck, hypertelorism, low-set ears, deafness, and thrombocytopenia or abnormal platelet function.
BHASKARA HOSPITAL
OBSTETRICIAN &GYNECOLOGIST
Kakatiya Medical College
M.D ( OB&GY )
National Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics
Super Specialist in Reproductive Endocrinology
AADESH MEDICAL COLLEGE
Associate Professor HEAD OF UNIT PAEDIATRIC
Dr SN Medical College Jodhpur
MD PAEDS
Dr KUTE HOSPITAL
Dr KUTE HOSPITAL
Govt. Medical College Miraj
D M &S
Sepuri Endocrine & Diabetes Centre
Consultant Endocrinologist & Diabetologist
Royal College of Physicians, United Kingdom
Masters in Clinical Endocrinology & Diabetology
Karajgaonkar Hospital
Consultant
Govt. Medical College, Aurangabad. Maharashtra
M.B.B.S, M.S. ( General Surgery), Ph.D ( Psychology)
Sepuri Endocrine & Diabetes Center
Chief Endocrinologist & Diabetologist for the Last 25 Years
Royal College of Physicians, United Kingdom
Masters Degree in Clinical Endocrinology & Diabetes
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