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+917597921472priyanshu82@gmail.comDepartment of Pediatric MedicineSMS Medical College, Jaipur

DR. PRIYANSHU MATHUR

(M.D Pediatrics, India)

Associate Professor
Department of Pediatric Medicine,
J K Lone Hospital,
SMS Medical College, Jaipur
Rajasthan, India
Dr. Priyanshu Mathur is a well-known Pediatrician and Rare Disorders expert in Jaipur, India. He has an excellent academic record. He was an outstanding student from the beginning. After his schooling at Jaipur, he completed MBBS from Vijayanagar Institute of Medical Sciences, Bellary, Karnataka. He was adjudged the best outgoing student of the year and awarded gold medals in Paediatric Medicine and Obstetrics and Gynaecology. Vice-Chancellor of Rajiv Gandhi University of Health Sciences, Karnataka felicitated him for his academic achievements.

Being a passionate learner, he pursued post-graduate studies leading to MD (Pediatrics) from Dr S. N. Medical College Jodhpur.

He is working as Associate Professor of Pediatric Medicine in JK Lone hospital, SMS Medical College, Jaipur. He is a soft-spoken, humble, astute physician with excellent clinical skills.  He has a vast experience in treating children. He is a favourite teacher amongst undergraduate and postgraduate students. He is also a keen researcher with more than twenty publications in national and international journals to his credit. He is also co-author of the book “Rare Diseases in Pediatrics”.

He has a particular interest in Pediatric Rare Disorders and Metabolic Genetic Disorders. He completed Indian Council of Medical Research Course in “Medical Genetics and Genetic Counseling” at  Sanjay Gandhi Post Graduate Institute, Lucknow. He received training in myopathies from Institut de Myologie, Paris, France.

He worked as a visiting assistant professor and did his one year training in metabolic genetics and newborn screening at the department of Human Genetics, Emory University school of medicine, Atlanta, Georgia, USA

Presently he is working in the department of pediatric medicine at J k Lone hospital, SMS Medical College, Jaipur as consultant Metabolic Genetics and running weekly Pediatric rare disease clinic.

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YEARS OF CONSULTATION

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PUBLICATIONS

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AWARDS

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SATISFIED FAMILIES

CREDITS & ACADEMIC BACKGROUND

  • Certifications
  • Awards
  • Research
  • Clinical Experience
  • Teaching Experience
  • Publications
  • Professional Memberships
  • Education

2022    Awarded Honorary Doctorate In Genetics by International Internship University

2017	Awarded Diploma in 20th Summer school of myology at Institut de Myologie, Paris, France

2017	Completed course on “Genomic and Precision Medicine” by University of California, San Francisco, USA

2015	Certified in Medical Genetics and Genetic Counselling, 14th ICMR Course,  SGPGI, Lucknow, India
2016	Awarded “Dakshata Praman Patra” at SMS Medical College, Jaipur, India

2009	Silver medal in paper presentation at State Pediatric conference held at Jaipur, India

2009	Won Divisional round of 3rd IAP Pediatric quiz for PG`s held at Jodhpur, India

2005	Secured 1st rank in final M.B.B.S. in VIMS, Bellary, Karnataka, India

2005	Awarded as Best outgoing student in VIMS, Bellary, Karnataka, India

2005	Awarded certificate of Merit by The BDCCI

2005	Felicitated by Vice Chancellor, RGUHS (on doctor`s day, by IMA Bellary branch)

2005	Awarded gold medal in for securing highest marks in pediatric medicine

2005	Awarded gold medal in for securing highest marks in OBG

2005	Won State round of 17th IAP Pediatric Quiz held at KIMS, Bangalore

National Task Force Member

  1. Guidelines for Management of SMA during COVID-19 pandemic and beyond

Advisory Board Member

  1. Rare Disease India Foundation
  2. “Finding Fabry”- A Virtual Advisory Board organized by Takeda India Medical
    Affairs
  3. Advisory board on Management of N-acetylglutamate synthetase (NAGS)
    deficiency (2019)
2018 - Present		Fellow, clinical biochemical genetics and newborn screening

2014 - 2018		Rare diseases clinic at J K Lone hospital, Jaipur, Rajasthan, India

2012 - 2018			Assistant Professor, SMS Medical College, Jaipur, Rajasthan, India

2010 - 2012		Senior Resident, SMS Medical College, Jaipur, Rajasthan, India

2007 - 2010		MD Pediatric Medicine, Dr. S. N. Medical College, Jodhpur, Rajasthan, India

2000 - 2005		MBBS, Vijayanagar Institute of Medical Sciences, Bellary, Karnataka, India
2018 - Present		Fellow, clinical biochemical genetics and newborn screening

2014 - 2018		Rare diseases clinic at J K Lone hospital, Jaipur, Rajasthan, India

2012 - 2018			Assistant Professor, SMS Medical College, Jaipur, Rajasthan, India

2010 - 2012		Senior Resident, SMS Medical College, Jaipur, Rajasthan, India

2007 - 2010		MD Pediatric Medicine, Dr. S. N. Medical College, Jodhpur, Rajasthan, India

2000 - 2005		MBBS, Vijayanagar Institute of Medical Sciences, Bellary, Karnataka, India
2019 - Present	    Associate Professor, SMS Medical College, Jaipur, Rajasthan, India

2012 - 2019		    Assistant Professor, SMS Medical College, Jaipur, Rajasthan, India

2010 - 2012	    Senior Resident, SMS Medical College, Jaipur, Rajasthan, India

2007 - 2010	    MD Pediatric Medicine, Dr. S. N. Medical College, Jodhpur, Rajasthan, India

Journal Reviewer

  1. Journal of Inherited Metabolic Disorders (JIMD)
  2. Indian Journal of Child Health (IJCH)
  3. Rajasthan Medical Journal (RMJ)
  4. BMC Medical Genomics

Journal Regional Editor:

  1. Archives of Practical Pediatrics

Original Articles

  1. Khandelwal S, Mathur P, Gupta ML. Prevalence of obesity and overweight in private schools of Jaipur city in 11-17 year age group children. Sch. J. App. Med. Sci., 2016; 4(4D): 1428-1432
  2. Bhargava M, Mathur P. Correlation study of various factors with germinal matrix-intraventricular hemorrhage in preterm neonates. Sch. J. App. Med. Sci., 2016; 4(4C): 1297-1301
  3. Gurjar M, Gupta A, Mathur P, Saroj AK. Evaluation of nutritional & educational intervention as KAP and outcome of children with SAM (6 Months – 5 years) in malnutrition treatment center. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS); Volume 15, Issue 6 Ver. III (June. 2016), PP 43-48
  4. Mathur P, Jain PK, Gupta BD. Chloroquine vs co-artemether in uncomplicated malaria. Sch. J. App. Med. Sci., 2016; 4(6B): 1981-1985
  5. Chonsariya R, Gupta A, Garg M, Mathur P, Khan K, Agarwal A. Comparison of risk factors and early morbidity in late preterm neonates and term neonates. Sch. J. App. Med. Sci., 2016; 4(8D): 2996-3001
  6. Choudhary K, Mathur P, Garg M, Gupta PP. Prevalence of impaired glucose tolerance test and diabetes in overweight, obese and apparently healthy school going adolescents. Int J Contemp Pediatr 2017; 4: 1081-87
  7. Choudhary K, Mathur P, Garg M, Gupta PP. Prevalence of overweight and obesity amongst adolescents and identification of risk factors. Int J Contemp Pediatr 2017;4:1153-9
  8. Bagri DR, Gupta RK, Mathur P. Assessment of parents and child’s attitude as barrier to dietary compliance in celiac disease. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS); Volume 15, Issue 8 Ver. VI (August. 2016), PP 53-58
  9. Khan K, Garg M, Sharma SD, Mathur P, Agarwal A. Study on clinical presentations, risk factors and short term outcome of hemorrhagic disease of newborn. Sch. Acad. J. Biosci., 2016; 4(8): 671-675
  10. Bilwal R, Mathur P. Epidemiological study of HIV-AIDS in children of western Rajasthan. Paripex-Indian J of research 2018;7(3):147-148
  11. Bagri DR, Gupta RK, Mathur P. Psychosocial Impacts as Predictors of Compliance in Celiac Disease. Indian Journal of Clinical Practice; 2018 Dec: 29(7): 637-641
  12. Mathur P, Agarwal A, Goyal K, Mathur A. Mutation spectrum of Duchenne muscular dystrophy patients in Indian population. Indian J Child Health. 2020; June 15 [Epub ahead of print]
  13. Singh H, Devpura K, Gothwal S, Nangliya V. L., Mathur P, Agarwal A. Study of Post Phototherapy Serum Bilirubin Rebound Levels in Near Term and Term Neonates. Sch J App Med Sci. 2020; June 20: 1502-1509 (Open Access)
  14. Sharma A, Mathur P, Sharma J N, Gupta M, Agarwal A. Neonatal Sepsis – A Study of Predisposing Factors and Causative Organisms. Sch J App Med Sci. 2020;2256-2259 (Open Access)
  15. Sharma A, Mathur P, Agarwal A, Gupta M. A Study of Predisposing factors for Fungal Sepsis and Causative Organisms. Sch J App Med Sci. 2020;2246-2250 (Open Access)

Case Reports

  1. Bagri DR, Gupta RK, Mathur P, Mittal R. Mermaid syndrome (sirenomelia): With use of mifepristone and misoprostol in early first trimester with failed medical abortion and continuing pregnancy in a multipara with bad obstetric history. Sch. J. App. Med. Sci., 2016; 4(5B): 1574-1576
  2. Bagri DR, Mathur P. P. vivax malaria: A rare cause of cholestatic jaundice in a neonate. Sch J Med Case Rep., 2016; 4(5): 315-317
  3. Pandit MS, Gupta A, Mathur P, Sharma M, Garg M. A case of Landau-Kleffner syndrome. J PediatrCrit Care 2016; 2: 61-63
  4. Gupta V, Gupta A, Mathur P, Sharma M, Garg M. Christ-Siemens-Touraine syndrome (X-linked hypohidrotic ectodermal dysplasia). Sch J Med Case Rep., 2016; 4(6): 379-381
  5. Pandit MS, Gupta A, Mathur P, Sharma M, Garg M, Kumar R. A case report of Kartagener syndrome. Sch J Med Case Rep., 2016; 4(6): 409-411
  6. Gupta V, Gupta A, Mathur P, Sharma M, Garg M, Kumar R. A rare case of Wegener’s granulomatosis with allergic bronchopulmonary aspergillosis in a child. J PediatrCrit Care 2016; 3
  7. Kumar R Gupta A, Mathur P, Sharma M, Garg M. Extensive mongolian spots: a clinical sign merits special attention for GM1-gangliosidosis. Int J Pediatr Res.2016; 3(7): 483-486 
  8. Garg M, Gupta A, Mathur P, Sharma M, Kumar R, Gupta V, Manjunath M. A rare case of glycogen storage disease type XI Fanconi-Bickel syndrome. J Pediatr Crit Care 2016; 3  
  9. Kumar R, Gupta A, Mathur P, Garg M. Factor XII deficiency – A rare coagulation disorder. Indian J Child Health 2016; 12
  10. Garg M, Kumar R, Mathur P, Gupta V. A case of atypical hemolytic uremic syndrome. Sch J Med Case Rep 2016; 4(7): 556-558
  11. Bansal N, Gupta A, Goyal M, Sharma M, Mathur P, Agarwal M. Oro facial digital syndrome type 2 – An Indian case report. J Pediatr Crit Care 2016; 3(4): 115-117
  12. Bagri DR, Sharma R, Mathur P. Autoimmune polyglandular syndrome Type IIIB associated with immune thrombocytopenia, leukopenia, beta thalassemia trait, and language impairment. J Diabetes Endocr Pract 2017; 1:9-11
  13. Gupta A, Mathur P, Sharma M, Parmar V. A case report of hypertension-short stature-brachydactyly (bilginturan) syndrome. The Rajasthan Medical J 2017; 1: 25-27 
  14. Goyal M, Gupta A, Sharma M, Mathur P, Bansal N. Fetal Valproate Syndrome with  Limb Defects: An Indian Case Report.Case Rep Pediatr. 2016;3495910
  15. Goyal M, Gupta A, Mathur P, Sharma M. Hypohidrotic Ectodermal Dysplasia: A rare case series. Journal of pediatric critical care; 2018: Vol. 5 – No.1 Jan-Mar
  16. Gupta A, Mathur P, Sharma M, Parmar V. A rare case of compound heterozygous B-thalassemia and hereditary persistence of fetal hemoglobin with Moya-Moya disease. Journal of Pediatric Critical Care; 2017; 4(3): 110-113
  17. Bagri DR, Jangid N, Sharma R, Mathur P. Pulmonary venous atresia-A rare and important etiology of recurrent LTRI. The RMJ 2018 Jan; 52-54
  18. Agarwal A, Goyal K, Mathur P, Minocha P, Bansal K, Mathur N. A rare mutation in alkaptonuria patients. Indian J Child Health. 2020; April 10 
  19. Agarwal A, Goyal K, Mathur P, Mathur A. Encephalopathy due to mutation in mitochondrial fission factor gene. Indian J Child Health. 2020; 7(4):184-187
  20. Agarwal A, Goyal K, Mathur P, Mathur A. A Rare case of Sanfilippo syndrome type “C.” Indian J Child Health. 2020; May 09 [Epub ahead of print]
  21. Gopaal N, Sharma JN, Mathur P, Agarwal V, Jadoun L. Neurofibromatosis type-1 with seizures and cerebrovascular malformation: A case study. Int J Contemp Pediatr 2020;7:1933-6
  22. Nagpal T, Agrawal K, Gupta A, Mathur P. Spinal muscular atrophy with progressive myoclonic epilepsy – rare case report from India. Int J Contemp Pediatr 2021;8:381-2
  23. Srinivas RK, Gupta A, Mathur P, Agarwal K, A. An infant with hypertriglyceridemia presenting as failure to thrive: a case report. Int J Contemp Pediatr 2021;8:590-3
  24. Gopaal N, Sharma JN, Agarwal V, Mathur P, Jadoun L. Congenital CMV Infection With CMV Pneumonitis’, International Journal of Current Medical and Pharmaceutical Research, 2020; 06(09), pp 5255-5258
  25. Agarwal A, Mathur P. Helsmoortel – Van Der AA Syndrome. International Journal of Scientific Research. March 2021: 10(03):2277 – 8179

Books Published

  1. Co-Author of A Textbook – Rare Diseases in Pediatrics 2nd edition printed in Feb 2016
  2. Contributed Chapter on Metabolic disorders in “Partha`s Comprehensive Manual for Pediatric and Adolescent Practice”
  3. Contributed Chapter on Metabolic disorders in “Partha`s Comprehensive Manual for Pediatric and Adolescent Practice”
  4. Contributed Chapter on Metabolic Disorders (Chapter 19) – Partha’s Current Trends in Diagnosis and Management in Pediatric and Adolescent Practice (PCTDMPAP)
  5. Editor of Atlas on Rare Diseases

Poster Presentations

  1. SSIEM 2019 – Evaluating Mental Health Outcomes in Patient Reported Outcomes Measurements Information System (PROMIS) in PKU
  2. RajPedicon 2019 – Recurrent Vomiting With Encephalopathy: Think Urea Cycle Defect (Won 1st prize)
  3. RajPedicon 2019 – Mutation Spectrum Of Duchenne Muscular Dystrophy (Dmd) Patients
  4. 2014 – Breastfeeding status report – India
  5. 2012 – Experience with BFM 95 protocol in acute leukemia in Asian children
2018 - Present		TREAT-NMD Alliance Neuromuscular Network, Europe

2017 - Present		ISIEM (Indian Society for Inborn Error of Metabolism)

2012 - Present		IMA (Indian Medical Association)

2011 - Present		NNF (National Neonatal Forum), India

2007 - Present	IAP (Indian Academy of Pediatrics)
2007 - 2010	MD Pediatrics, Dr. S. N. Medical College, Jodhpur, Rajasthan, India

2000 - 2005	MBBS, Vijayanagar Institute of Medical Sciences, Bellary, Karnataka, India

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