Meet Our Doctors
Dr. Anil Bansidhar Jalan
Paediatrics
Registration No
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Years of Experience
24 years
Languages
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Degree
M.B.B.S., D.C.H, M.D(Paedicatrics)
Specialty and Areas of Interest
- Inborn Errors of Metabolism in critically ill Newborns.
- Inborn Errors of Metabolism in Sudden Infant Death Syndrome (SIDS).
- IEM and other genetic defects in recurrent abortions or fetal losses / bad obstetric history cases.
- IEM and other genetic disorders in mentally and physically handicapped children
- Genetics of hearing deficit and other neurological defects.
- Genetics of multiple congenital anomalies and their prenatal diagnosis.
- Autism and Attention Deficit Hyperactivity Disorders (ADHD)
- Prader Willi Syndrome
Achievements
- Paper presented at national ISPAT Conf (Indian Society for Prenatal Diagnosis and Therapy) - 2006 1. Tyrosinemia Type I: Clinical, Biochemical and molecular profile of Indian patients.
- Poster presentation at 3rd International Neurocon conf. (Paediatric neurology) at Chandigarh - 30th Oct. to 15 Nov. 2009. Abstract book - Paediatric Neurology & Epilepsy, Editor - Prof. Pratibha Singhi
- Intracellular Gluathione status in metabolic encephalopathies, Abstract Book, NEU/NM-1, Pg 168
- Leukoencephalopathies Associated with Inborn error of Metabolism, Abstract Book, NEU/NM-2, Pg 168
- Lecture taken at "Pedgastro Conf 2011" National Gastroenterology Conf. at Gurgaon 46th Nov. 2011: Metabolic Liver Diseases approach to diagnosis.
Professional membership and certification
- Currently holding the post of Chief Scientific Research Officer at NIRMAN (Navi Mumbai Institute of Research in Mental and Neurological Handicap).
- Freelance visiting Paediatric Geneticist and expert in metabolic disorders of children, especially critically ill newborns, to various hospitals.
- Received formal and advanced training in Laboratory Techniques in Inborn Errors of Metabolism at CDFD (Center for DNA Finger Printing and Diagnostics, Hyderabad, India).
- Received advanced training in Laboratory techniques in Inborn Errors of metabolism and mass-scale newborn screening at various European Universities and Clinics.
Research & Publications
- Arthrogryposis"- Bio Med., July 1999 issue.
- Neonatal Hyper-lysinemia - A Cause of Severe Birth Asphyxia", Paper submitted in IAP-Mumbai conference, Oct. 1999, Pg. FP-1-10.
- Non-Immune Hydrops Foetails" - Bio Med., Dec. 1999, Pg. 128-132.
- SIDS, A Composite of Doom-Bio Med., Feb. 2000 issue Pg. 32-34. 5. "Sudden Infant Death Syndrome" - Perinatology, 2000, Vol: 2 Number 4, Pg. 177-186.
- Thyroid Function Tests in Sick Neonates" - Perinatology 2000, Vol. 2 Number 6, Pg. 265-274.
- Inborn Errors of Metabolism in Critically ill Newborns - Part 1
- Perinatology 2001, Vol. 3, No.1: Pg. 13-24. 8. "Inborn Errors of Metabolism in Critically ill Newborns - Part II
- Perinatology 2001. Vol. 3 and No. 3: Pg. 113-121. 9. 3-Hydroxy-3-Methylglutaric Aciduria (HMG Co A Lyase deficiency)
- Quarterly journal of Mumbai IAP Brach-Impression" - Vol.1 Issue No. 2, July 2001; Pg. 16-23.
- Neonatal Metabolic and Genetic Disorders, a book on Genetic and metabolic disorders for Pediatricians and Gynecologists, published in Jan. 2000.
- Toxoplasmosis Perinatology Vol. 4 (2): 75-83.
- Newborn Screening in India" Presented a Research Paper at the National Conference of ISPAT at Pune - Jan. 2002.
- Biotinidase deficiency - screening in High risk newborn and pediatric population of India." Research paper accepted for presentation at International Conference of Newborn Screening was held in Italy from 25th June-29 June 2002.
- Newborn Screening for Galactosemia". Thesis completed by M.Sc. Student under my supervision at our center.
- Biochemical Parameters of Mental Retardation - Use of Ammonia as a screening procedure." Thesis completed by an M.Sc. (Research) Student of Bombay University under my supervision at our center.
- VLCAD deficiency A. B. Jalan and B. Awasthi, Perinatology, Vol. 6 (4), July-Aug. 2004; 197-202
- Galactosemia", Journal of Genetics, Screening and Health, Vol1 No.2- June 2006: 33-44.
- Biotinidase Deficiency Urgent Need for Newborn Screening in India. Journal of Genetics, Screening, and Health, Vol 1 No 3-Nov 2006. 20. Fructose 1, 6 Diphosphatase Deficiencies, Journal of Genetics, Screening, and Health, Vol 2 No 2-Apr-May-June 2007.
- Incidence of Preventable IEM in Indian Children with mental Retardation" Journal of Genetics, Screening, and Health, Vol 3 No 1 Jan-Feb-Mar 2008.
- Outcome and Management of Citrullinemia in Indian Society" Journal of Genetics, Screening and Health, Vol.3 No. 2 Oct-Dec 2008, 22-32
- Outcome of VLCAD Deficiency in Indian newborns Perinatology 2009 Vol 11 (2): 99-104.
- Newborn Screening," Rajneocon - 09, "Comprehensive Neonatal Care Souvenir: 2010, Pg 1-12
- Outcome of MSUD in Indian Neonates Journal of Genetics Screening and Health, Vol-4 No. 1-Jan 2010; 38-45,
- Understanding GC-MS-a Chapter contributed to a Textbook of Medical Genetics (in Press).
- Etiology and outcome of Inborn Errors of Metabolism." Shehla Choudhary, Masood Khan, Hani Akbar Rao, Anil Jalan and Ejaz Khan, J Pak Med Assoc, JPMA 63: 2013: 1112-1116.
- Management of Urea Cycle defects in a Developing Country, Journal of Paediatric Riechemisto: 4/2014) 1-6 DOI 10.3233 / IPB 140101 IOS.