Dr. Ruchi R Parikh

Dr. Ruchi R Parikh

Paediatrics, Paediatrics / Endocrinology

M.B.B.S., DNB (PEDS), FELLOWSHIP IN PEDIATRIC ENDOCRINOLOGY

Profile

Dr. Ruchi Parikh has been a valued member of the Lilavati Hospital team since February 2020. She brings extensive experience of over 8 years and has provided care for more than 3,500 children as a Pediatric and Adolescent Endocrinologist.

Her advanced training and experience include:

  • European Society of Pediatric Endocrinology (ESPE) Clinical Fellowship in the Department of Pediatric Endocrinology, Alder Hey Children’s Hospital, Liverpool, United Kingdom (May 2018 – August 2018).
  • International Observer Program, Division of Endocrinology and Diabetes, Children’s Hospital of Philadelphia, USA (September 2017 – November 2017).
  • Participation in the 1st APPES & APEG (Asia Pacific Pediatric Endocrine Society & Australasian Pediatric Endocrine Group) Joint Fellows School, representing India, Darwin, Australia, 2014.

Her accomplishments include:

  • Executive Member, Indian Society for Pediatric & Adolescent Endocrinology (ISPAE) (2019-2020).
  • Coordinator, Pre PEDICON 2019 Endocrinology Workshop, BJWHC, Mumbai.
  • Organizing Committee Member, ISPAE-ISPAD 2016, Sugars & Beyond, Midterm Meeting, Nashik.
  • Conducted Growth Camps.
  • Participated in the 3rd Biennial Conference of ISPAE-PET, Bengaluru.

She has presented posters and cases at various state, national, and international conferences, including:

  • IAP, India
  • ISPAE, India
  • IMPE, USA
  • ESPE, Europe
  • APPES-APEG, Australia
  • BSPED, UK

Areas of Interest (in children aged 0-18 years):

  • Growth Disorders: Short Stature and Obesity (Metabolic syndrome)
  • Thyroid Disorders
  • Pubertal Disorders: Early and Late
  • Diabetes Mellitus in children: Type 1 (Juvenile), Type 2 (Insulin resistance), and Neonatal
  • Hypoglycemia (Low Blood Glucose)
  • Long-term endocrine effects in survivors of hemato-oncological disorders (Thalassemia, Malignancy, etc.) and chronic systemic illness
  • Disorders of Calcium, Vitamin D, and Bones
  • Disorders of Sex Development (Atypical genitals)
Awards & Recognition

Recognitions:

  • Member, National Executive Board, Indian Society for Pediatric & Adolescent Endocrinology (ISPAE) (2019-2020).
  • Member, Indian Society for Pediatric and Adolescent Endocrinology (ISPAE).
  • Member, International Society for Pediatric and Adolescent Diabetes (ISPAD).
  • Member, Asia Pacific Pediatric Endocrine Society (APPES).
  • Member, Growth Hormone Research Society (GHRS).
  • Member, Indian Academy of Pediatrics (IAP).
  • Member, Indian Medical Association (IMA).
  • Frequent Faculty Speaker at state, national, and institutional Pediatric and Pediatric Endocrinology CMEs and conferences.
  • Provides instruction and training to Pediatric and Pediatric Endocrinology trainees at various institutions.

Awards:

  • Awarded Best Clinical Case Presentation, “Breakout sessions on Transition and Adult Growth Hormone Deficiency,” at the Inaugural Endocrinology Academy Meeting “Bridging Paediatric and Adult Endocrine Disorders,” London, UK (2018).
  • Awarded 2nd Position, Indian Journal of Pediatrics-Competitive Grand Rounds 2014, for the case presentation “Unusual Cause of Hypocalcemic Convulsions: Hypomagnesemia with Secondary Hypocalcemia (HSH)” at AIIMS, Delhi.
  • Achieved Distinctions in Biochemistry and Ophthalmology during MBBS training.
Research Publications
  • M.P. Desai, R. Sharma, I. Riaz, S. Sudhanshu, R. Parikh, V. Bhatia. "Newborn Screening Guidelines for Congenital Hypothyroidism in India: Recommendations of the Indian Society for Pediatric and Adolescent Endocrinology." Indian J Pediatr. 2018 Jun;85(6):440-447 & Indian J Pediatr. 2018 Jun;85(6):448-453.
  • Shah R, Rao S, Parikh R, Sophia T, Khalid H. "Fanconi Bickel Syndrome with hypercalciuria due to GLUT 2 Mutation." Indian Pediatr. 2016 Sep 8;53(9):829-830.
  • Singh P, Rao SC, Parikh R. "Neonatal Diabetes with intractable Epilepsy: DEND Syndrome." Indian J Pediatr. 2014 Dec;81(12):1387-8.
  • Daphne Y, Kevin C, Anuja N, Ruchi P, Natalie C, Mohammed D, Senthil S, Indraneel B. "Congenital Hyperinsulinism due to mutations in HNF1A." Accepted for publication in European Journal of Medical Genetics, April 2020.
  • Article on McCune Albright Syndrome published in CAPENEWS, Newsletter of ISPAE, September 2014, Volume 18, Issue 2, pages 6-8.
  • Chapter Author, “Hypoglycemia in an Older child,” IAP Textbook of Pediatric Endocrinology, Vaman Khadilkar, Anurag Bajpai, Hemchand Prasad. Released in 2019. Chapter 46.
  • Chapter Author (with Dr. Meena Desai), “Normal Puberty,” Disorders of the Endocrine Gland for the Postgraduate Textbook of Pediatrics, Piyush Gupta, PSN Menon, Siddarth Ramji, Rakesh Lodha. Released in 2015. Chapter 44.10, Sec-44 (1-33).indd 2326-2330.
  • Chapter Author (with Dr. Meena Desai), “Disorders of Thyroid Gland,” IAP Textbook of Pediatrics 7th Edition, Piyush Gupta, PSN Menon. Chapter 13.5.
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