Dr. Ranjana Mishra

About  Dr. Ranjana Mishra

Dr. Ranjana Mishra, a seasoned professional, brings over 17 years of remarkable experience in obstetrics and gynecology across private, government, and defence sectors. Her practice took a unique turn with over 5 years of expertise in medical genetics, adding a distinctive dimension to her approach.

As a dedicated medical geneticist, Dr. Mishra plays a pivotal role in early screening of genetic diseases as well as in redefining women's health, seamlessly combining precision and care in every aspect.

Educational Qualifications

Educational Qualifications

• M.B.B.S, Motilal Nehru Medical College, Allahabad
• D.G.O, King George's Medical College, King George's Medical University, Uttar Pradesh
• D.N.B (Obstetrics & Gynaecology), Army Hospital R&R, Delhi
• D.N.B-SS (Medical Genetics), Sir Gangaram Hospital, New Delhi

Experiences

• Senior Resident (O&G), Sitaram Bhartia Institute of Science & Research, Delhi- Feb. 2004 - Apr. 2005
• Senior Resident (O&G), Sardar Vallabh Bhai Patel Hospital (GNCT), Delhi- May 2005 - Jul. 2005 & May 2007 - Jul. 2010
• Medical Officer (O&G), Sardar Vallabh Bhai Patel Hospital (GNCT), Delhi - Oct. 2010 - May. 2017
• Junior Research Fellow (JRF), ICMR Project (National Registry for Rare and Other Inherited Disorders), Sri Gangaram Hospital - Dec. 2020 - Mar. 2021
• Senior Medical Officer, Thalassemia Screening Program, Maulana Azad Medical College & Associated Lok Nayak Hospital
• Senior Consultant, Medical Genetics Yashoda Hospital & Research Centre, Nehru Nagar, Ghaziabad - 2023 - Present

Specializations

• Diagnosis & management of genetic disorders like genetic syndromes & inborn errors of metabolism
• New born screening & genetic diagnostics
• Analysis, work-up & counselling of familial genetic disorders like hereditary cancers, neurodegenerative disorders like Huntington's disease & intellectual disability like Fragile X
• Pre-conceptional genetic counselling in case of recurrent pregnancy loss, previous stillbirth, one parent with a known genetic disease, congenital anomaly or developmental disorders, prior child with a known genetic disease/congenital anomaly or developmental disorder, family history of genetic disease teratogen exposure, consanguinity & infertility
• Fetal medicine counselling for fetal malformations, aneuploidy screen & prenatal genetic diagnosis
• Genetic evaluation of developmental delays, intellectual disability, epilepsies & neuromuscular disorders
• Genetic evaluation of congenital malformations/birth defects like congenital heart disease, cleft lip/palate, neural tube defect & renal anomalies

Accomplishments & Awards

• Presented paper titled 'Medical Abortion: A Safe and Reliable Option for Early MTP' at the 27th Annual Conference of AOGD, 5-6 November 2005
• Presented poster on 'Fabry Disease: An Underdiagnosed Entity with Variable Clinical Presentation' at the 3rd South-Asia & 19th Asia LSD symposium, New Delhi, 2018
• Presented poster entitled 'Fabry Disease: Lessons Learnt' at the Fabry Expert Lounge at Dubai, UAE, 21- 22 September, 2018
• Changing Practices in Genodermatosis, 4th International Conference on Birth Defects and 5th Annual Conference at the Society of the Indian Academy of Medical Genetics, Vellore, Tamil Nadu, December 2018
• 'Clinical, Biochemical & Molecular Spectrum of Disorders of Carbohydrate Metabolism: The Sweet Story, 5th National Conference, Indian Society of Inborn Errors of Metabolism, Pune, January 2019
• Oral paper entitled 'Robinow Syndrome and Brachydactyly: An Interplay of High-Throughput Sequencing and Deep Phenotyping in a Kindred', at the 7th International Conference on Rare and Undiagnosed diseases, Gurgaon, 13-15 April 2019
• Presented poster entitled 'COASY Gene in Pontocerebellar Hypoplasia Series: The New Kid on the Block' at the Indo-US Symposium on Genetic Neuromuscular Disorders & Sixth Annual Conference of the Society for Indian Academy of Medical Genetics (SIAMGCON), 21-23 November 2019, Hyderabad
• Presented poster entitled 'Shwachman-Diamond Syndrome in 2 Siblings Mimicking as Cystic Fibrosis' at the 5th National Conference of the Indian Society of Primary Immune deficiency, Lucknow- March 6-7, 2021
• Presented poster entitled 'A Step-Wise Diagnostic Approach to Genetic Factors in Early Fetal Growth Restriction: A Pilot Study from India' at the 23rd International Conference on Prenatal Diagnosis and Therapy, Singapore, 8-11 September 2021

Research & Publications

• Mishra R., et al. 'Robinow Syndrome and Brachydactyly: An Interplay of High- Throughput Sequencing and Deep Phenotyping in Kindred' Mol Syndromol. 2020; 11:43-49. doi:10.1159/000505506.
• Mishra R., et al. 'Hypoxic ischemic encephalopathy, or metabolic etiology-MRI as a clue to diagnosis', Neurol India. 2020;68:941-42. doi: 10.4103/0028-3886.293478.
• Mishra R., et al. 'Gaucher Disease in Fetus: The Usual and the Unusual Presentations in a Family', J Fetal Medicine. 2019; 6(1-2). doi: 10.1007/s40556-019- 00216.
• Mishra R., et al. 'The Fatal Fetal Tumor: A Geneticist's Perspective', J Matern Fetal Neonatal Med. 2019 Jun 3:1-3. doi: 10.1080/14767058.2019.1622671.
• Mishra R., et al. 'Early Infantile Thiamine Transporter-2 Deficiency with Epileptic Spasms-A Phenotypic Spectrum with a Novel Mutation', Journal of Pediatric Epilepsy 2021; 10(04): 168-174. DOI: 10.1055/s-0041-1731018.
• Mishra, R., et al. 'Rapid Detection and Treatment of Inborn Errors of Metabolism in the Newborn Period: Beginning of a New Trend', Indian J Pediatr 88, 433-434 (2021). DOI:10.1007/s12098-021-03739-z.
• Mishra R., et al. 'Biotin Supplementation in Children with Symptomatic Profound Biotinidase Deficiency and Their Pregnant Mothers', Indian Pediatr Case Rep 2022;2:12-6. DOI: 10.4103/ipcares.ipcares_12_22.
• Mishra R., et al. 'COASY Related Pontocerebellar Hypoplasia Type 12: A Common Indian Mutation with Expansion of the Phenotypic Spectrum', Am J Med Genet A. 2022;188(8):2339-2350. doi:10.1002/ajmg.a.62768.
• Book chapters, Fatty Oxidation Defects. PG Textbook of Pediatrics, 3rd ed. Jaypee Brothers, 2022.