We are specialize in Pediatric
Rare Disease and
Consultant Metabolic Genetics

Dr. Priyanshu Mathur is a well-known Pediatrician and Rare Disorders expert in Jaipur, India. He was adjudged the best outgoing student of the year and awarded gold medals in Paediatric Medicine and Obstetrics and Gynaecology. He is also a keen researcher with more than twenty publications in national and international journals.

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
2005 Awarded certificate of Merit by The BDCCI
2005 Awarded gold medal in for securing highest marks in pediatric medicine
2005 Awarded gold medal in for securing highest marks in OBG

2018 – Present Fellow clinical biochemical genetics and newborn screening
2018 – 2018 Started NBS lab at J K Lone hospital, Jaipur, Rajasthan, India
2016 – Present Started first Indian Rare Diseases Registry (www.rarediseasesregistryindia.com)

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

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. 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
4. 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
5. Pandit MS, Gupta A, Mathur P, Sharma M, Garg M. A case of Landau-Kleffner syndrome. J PediatrCrit Care 2016; 2: 61-63
6. 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
7. Gupta V, Gupta A, Mathur P, Sharma M, Garg M. Christ-seimmens-touraine syndrome (X-linked hypohidrotic ectodermal dysplasia). Sch J Med Case Rep., 2016; 4(6): 379-381
8. Mathur P, Jain PK, Gupta BD. Chloroquine vs co-artemether in uncomplicated malaria. Sch. J. App. Med. Sci., 2016; 4(6B): 1981-1985
9. 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
10. Jora R, Mathur P, Gupta M, Chauhan H. A study of risk factors for LBW, VLBW & ELBW babies in western Rajasthan. Current Medical Trends., 2012;16: 2744-51
11. 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
12. Gupta V, Gupta A, Mathur P, Sharma M, Garg M, Kumar R. A rare case of Wegeners granulomatosis with allergic bronchopulmonary aspergillosis in a child. J Pediatr Crit Care 2016; 3
13. 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
14. 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
15. Kumar R, Gupta A, Mathur P, Garg M. Factor XII deficiency – A rare coagulation disorder. Indian J Child Health 2016; 12
16. 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
17. 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
18. 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
19. 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
20. 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

Books published

1. Co-Author of A Textbook – Rare Diseases in Pediatrics 2nd edition printed in Feb 2016.

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)

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