Dr. Arun Kumar Choudhury

Dr. Arun Kumar Choudhury

Associate Professor

Dr. Arun Kumar Choudhury

Associate Professor
Email: drarun39@yahoo.com
Permanent Address: Junuspatna,Ifo Bombay Hotel College Square, Cuttack-753003
Correspondence Address: Junuspatna,Ifo Bombay Hotel College Square, Cuttack-753003
Course Name Name of PG Degree Area of Specialization/ Specialty Year of Qualifying degree Name of University / Institute
MBBS 1993 UTKAL UNIVERSITY /SCB MEDICAL COLLEGE
PG Degree MD GENERAL MEDICINE 1998 UTKAL UNIVERSITY /SCB MEDICAL COLLEGE
Post Doctoral Qualification DM ENDOCRINOLOGY 2005 MUMBAI UNIVERSITY
  1. Mangaraj S, Mishra I, Patnaik AP, Choudhury AK, Baliarsinha AK. Neurofibromatosis Masquerading as Disorder of Sex Development. Indian J EndocrinolMetab. 2019 Sep-Oct;23(5):588-589. doi: 10.4103/ijem.IJEM_332_19. PMID: 31803604; PMCID: PMC6873258.
  2. Mangaraj S, Choudhury AK, Mohanty BK, Baliarsinha AK. Hypothyroidism masquerading as ovarian malignancy. J Paediatr Child Health. 2015 Sep;51(9):942-3. doi: 10.1111/jpc.12996. PMID: 26333086.
  3. Mangaraj S, Choudhury AK, Swain BM, Sarangi PK, Mohanty BK, Baliarsinha AK. Evaluation of Vitamin D Status and its Impact on Thyroid Related Parameters in New Onset Graves’ Disease- A Cross-sectional Observational Study. Indian J EndocrinolMetab. 2019 Jan-Feb;23(1):35-39. doi: 10.4103/ijem.IJEM_183_18. PMID: 31016150; PMCID: PMC6446662.
  4. Mangaraj S, Patro D, Choudhury AK, Baliarsinha AK. A rare case of acromegaly and autosomal dominant polycystic kidney disease: case report and brief review of literature. AACE Clin Case Rep. 2019 Jun 7;5(5):e302-e306. doi: 10.4158/ACCR-2019-0128. PMID: 31967058; PMCID: PMC6876956.
  5. Mangaraj S, Mishra PK, Choudhury AK, Mohanty BK, Baliarsinha AK. Prolactinoma Presenting as Short-lasting Unilateral Neuralgiform Headache Attacks with Conjunctival Injection and Tearing Syndrome. J Neurosci Rural Pract. 2017 Aug;8(Suppl 1):S158-S161. doi: 10.4103/jnrp.jnrp_37_17. PMID: 28936102; PMCID: PMC5602252.
  6. Mangaraj S, Choudhury AK, Singh M, Patro D, Baliarsinha AK. Spondylocarpotarsalsynostosis syndrome. A rare case of short stature and congenital scoliosis. Clin Cases Miner Bone Metab. 2017 May-Aug;14(2):258-261. doi: 10.11138/ccmbm/2017.14.2.258. Epub 2017 Oct 25. PMID: 29263747; PMCID: PMC5726223.
  7. Jena D, Choudhury AK, Mangaraj S, Singh M, Mohanty BK, Baliarsinha AK. Study of Visceral and Subcutaneous Abdominal Fat Thickness and Its Correlation with Cardiometabolic Risk Factors and Hormonal Parameters in Polycystic Ovary Syndrome. Indian J EndocrinolMetab. 2018 May-Jun;22(3):321-327. doi: 10.4103/ijem.IJEM_646_17. PMID: 30090722; PMCID: PMC6063187.
  8. Mangaraj S, Choudhury AK, Mohanty BK, Baliarsinha AK. Neurological manifestations of Graves’ disease: A case report and review of the literature. J Neurosci Rural Pract. 2016 Jan-Mar;7(1):153-6. doi: 10.4103/0976-3147.165393. PMID: 26933368; PMCID: PMC4750319.
  9. Dash DK, Choudhury AK, Singh M, Mangaraj S, Mohanty BK, Baliarsinha AK. Effect of parental history of diabetes on markers of inflammation, insulin resistance and atherosclerosis in first degree relatives of patients with type 2 diabetes mellitus. Diabetes MetabSyndr. 2018 May;12(3):285-289. doi: 10.1016/j.dsx.2017.12.004. Epub 2017 Dec 15. PMID: 29275995.
  10. Mangaraj S, Choudhury AK, Mohanty BK, Baliarsinha AK. A Case of Persistent Polyuria in an Insulin- Dependent Child With Diabetes. Clin Diabetes. 2016 Apr;34(2):109-12. doi: 10.2337/diaclin.34.2.109. PMID: 27092022; PMCID: PMC4833486.
  11. Agrawala RK, Choudhury AK, Mohanty BK, Baliarsinha AK. Perrault syndrome with growth hormone deficiency: a rare autosomal recessive disorder. J PediatrEndocrinolMetab. 2015 Sep;28(9-10):1005-7. doi: 10.1515/jpem-2014-0292. PMID: 25741941.
  12. Agrawala RK, Choudhury AK, Mohanty BK, Baliarsinha AK. All males do not have 46 xy karyotype: A rare case report. Indian J EndocrinolMetab. 2013 Oct;17(Suppl 1):S271-3. doi: 10.4103/2230-8210.119603. PMID: 24251184; PMCID: PMC3830330.
  13. Agrawala RK, Choudhury AK, Mohanty BK, Baliarsinha AK. Berardinelli-Seip congenital lipodystrophy: an autosomal recessive disorder with rare association of duodenocolonic polyps. J PediatrEndocrinolMetab. 2014 Sep;27(9-10):989-91. doi: 10.1515/jpem-2013-0399. PMID: 24825083.
  14. Agrawala RK, Sahoo SK, Choudhury AK, Mohanty BK, Baliarsinha AK. Pigmentation in vitamin B12 deficiency masquerading Addison’s pigmentation: A rare presentation. Indian J EndocrinolMetab. 2013 Oct;17(Suppl 1):S254-6. doi: 10.4103/2230-8210.119591. PMID: 24251178; PMCID: PMC3830324.