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INTERNATIONAL JOURNAL OF CREATIVE RESEARCH THOUGHTS - IJCRT (IJCRT.ORG)
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ISSN Approved Journal No: 2320-2882 | Impact factor: 7.97 | ESTD Year: 2013
Call For Paper - Volume 12 | Issue 6 | Month- June 2024
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Published Paper Details:
Paper Title
NOONAS SYNDROME
Authors
V.YASODHA
Keywords
: Autosomal dominant RASOPATHY , HETROGENUS
Abstract
Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations Facial features include widely spaced eyes, light colored eyes, low set ears, a short neck, and a small lower jaw Heart problems may include pulmonary valve stenos is The breast bone may be either protruding or be sunk while the spine may be abnormally curved Intelligence is often normal. Complications of NS may include leukemia
IJCRT's Publication Details
Unique Identification Number - IJCRT2103621
Paper ID - 203750
Page Number(s) - 5289-5295
Pubished in - Volume 9 | Issue 3 | March 2021
DOI (Digital Object Identifier) -
Publisher Name - IJCRT | www.ijcrt.org | ISSN : 2320-2882
E-ISSN Number - 2320-2882
Cite this article
V.YASODHA, "NOONAS SYNDROME", International Journal of Creative Research Thoughts (IJCRT), ISSN:2320-2882, Volume.9, Issue 3, pp.5289-5295, March 2021, Available at :http://www.ijcrt.org/papers/IJCRT2103621.pdf
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Volume 12 | Issue 6
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ISSN: 2320-2882 Impact Factor: 7.97 and ISSN APPROVED Journal Starting Year (ESTD) : 2013
ISSN and 7.97 Impact Factor Details
ISSN: 2320-2882 Impact Factor: 7.97 and ISSN APPROVED Journal Starting Year (ESTD) : 2013
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Scholarly open access journals, Peer-reviewed, and Refereed Journals, Impact factor 7.97 (Calculate by google scholar and Semantic Scholar | AI-Powered Research Tool) , Multidisciplinary, Monthly, Indexing in all major database & Metadata, Citation Generator, Digital Object Identifier(DOI)
