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Dr. Ashok Gupta

Prof. & HoD

Paediatrics

Currently working as senior professor & head of department of Paediatric medicine and incharge rare disease clinic at mahatma gandhi medical college and hospital jaipur. Currently the executive director of International neonatology association, geneva and chairpersonTechnical committee government of rajasthan on rare diseases. Has been on the board of the international paediatric association And the president of the international society of tropical paediatrics. Also been on the editorial board of the journal of tropical paediatrics-Oxford university.

Press and the advisory board member of the indian Paediatrics and the indian journal of practical paediatrics. Recipient of the fellowship from the american academy of paediatrics Vide india gyani fund, rotatory foundation fellowship and neonatal Visiting fellowship from university of illinosis of chicago

Experience

Qualification

MBBS /MD

    • Invited as national speaker by government of Izrail to talk over national policy of Rare disease in Nov 2019.
    • Nominated as one of the members of the National policy advisory committee for Rare disease, government of India.
    • Chairman of National committee for National policy for treatment of Rare diseases for Rajasthan.
    • One of the board members of Asian alliance on Food allergy, Tokyo.
    • Governing board member of European academy taskforce on Food allergy.
    • Chairperson Rare disease taskforce Asia pacific pediatric society.
    • Executive director of international neonatology associations (Geneva).
    • Course director food allergy, European academy Munich meetings.
    • Received education grant for abstract titled Hereditary fructose intolerance: unusual findings in a genotypic confirmed case in Asia Pacific digestive week (APDW 2019) at Kolkata 12-15 Dec2019.
    • Oration over Epigenetics in pediatrics in Rajpedicon 2019.
    • Organized one day Symposium over MPS – Diagnosis and management on 11 Dec 2019.
    • Invited as a speaker to talk over Mucopolysacharidosis Indian perspective in 1st Asia/Middle East MPS Preceptorship Program: MPS Disease Diagnosis, Management and Treatment. 18-19 Oct 2018 Taiwan.
    • Poster presentation titled Hypotonia diagnostic challenges in Westneocon Nov 2019 Jaipur.
    • One of the team members (Dr. Manisha Goyal) was facilitated by Rajasthan medical council for her work and research papers on genetics July 2017.
    • Actively participated PIDCON 2018 (Primary immunodeficiency diseases national conference, held on 10-11th March Jaipur).
    • Faculty talk over MPS diseases in Genetic and rare diseases in Medical practice: How to recognize and manage, Feb 2018 in Jaipur.
    • Poster presentation in 3rd South Asia and 19th Asia LSD symposium from 20th - 22nd April 2018 in New Delhi titled Mucopolyscharidosis.
    • Oral presentation in 3rd South Asia and 19th Asia LSD symposium from 20th - 22nd April 2018 in New Delhi titled “Skeletal manifestations in Gaucher Disease type 1”.
    • One of the team member invited as a speaker to share experience over MPS Perspective in 1st Asia/Middle East MPS Preceptorship Program: MPS Disease Diagnosis, Management and Treatment. 18-19 Oct 2018, Taipei Taiwan.
    • Poster presentation in annual conference of Indian Radiological and imaging association, at Jaipur in January 2017, titled” Schmid type of Metaphyseal Chondrodysplasia: phenotype and genotype features.
    • Poster presentation Cancer Genetics in 1st International conference on rare disease at Jaipur, Nov 2017.
    • Oral presentation in birth defect conference at New Delhi, Nov. 2016, titled ‘Lethal osteogenesis imperfect: Recurrence in an Indian family’.
    • Participated preconference Genetic workshop titled “Genetic Disorders: Clinical and laboratory diagnosis and management” on 27 Nov 2015 in 1st International conference on rare disease at Jaipur.
    • Awarded second place in the poster presentation in 1st International conference on rare disease at Jaipur, Nov. 2015, titled “Genotypically confirmed Stickler syndrome with unusual eye findings”.
    • Poster presentation in 1st International conference on rare disease at Jaipur, Nov. 2015, titled ‘Apert syndrome with preaxial polydactyly: An unusual feature’.

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Mahatma Gandhi University of Medical Sciences & Technology

Sitapura, Tonk Road, Jaipur, Rajasthan (India) – 302022