Volume : VII, Issue : II, February - 2018

A case of Noonan syndrome

Dr. Bhargavan Pallivalappil, Dr. Shiji Pallivalappil, Dr. Avinash Sarpamale, Dr. Ramesh Naga Supreeth, Dr. Hariprasad Imandi

Abstract :

 Noonan syndrome is a type of genetic disorder with wide variety of clinical features. Sometimes diagnosis may be difficult at early stage. We describe a case of 32 year old male with anaemia associated facial dysmorphism, short stature and hypertrophic cardiomyopathy. Genetic screening of this patient also has been tried. At present patient is being managed symptomatically

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Article: Download PDF   DOI : 10.36106/ijsr  

Cite This Article:

Dr. Bhargavan Pallivalappil, Dr. Shiji Pallivalappil, Dr. Avinash Sarpamale, Dr. Ramesh Naga Supreeth, Dr. Hariprasad Imandi, A case of Noonan syndrome, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-7 | Issue-2 | February-2018

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