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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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
Number of Downloads : 489
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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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