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Dr. Dhanya Yesodharan

Professor, Department of Paediatrics, School of Medicine, Kochi

Qualification: MD
dhanyayesodharan@aims.amrita.edu

Bio

Dr. Dhanya Yesodharan currently joined as Professor at the Department of Paediatrics, School of Medicine, Kochi.

Languages Known

  • English
  • Malayalam
Publications

Journal Article

Year : 2018

Elsahy-Waters syndrome is caused by biallelic mutations in CDH11.

Cite this Research Publication : F. L. Harms, Nampoothiri, S., Anazi, S., Dhanya Yesodharan, Alawi, M., Kutsche, K., and Alkuraya, F. S., “Elsahy-Waters syndrome is caused by biallelic mutations in CDH11.”, Am J Med Genet A, vol. 176, no. 2, pp. 477-482, 2018.

Publisher : Am J Med Genet A

Year : 2017

Plexiform Neurofibroma of Clitoris.

Cite this Research Publication : Dhanya Yesodharan, Sudarsanan, B., Jojo, A., Abraham, M., Bhavani, N., Mathews, H., and Nampoothiri, S., “Plexiform Neurofibroma of Clitoris.”, J Pediatr Genet, vol. 6, no. 4, pp. 244-246, 2017.

Publisher : J Pediatr Genet

Year : 2016

Sirenomelia: Case reports and current concepts of pathogenesis

Cite this Research Publication : Ma Pillay, Yesodharan, Db, Narayanan, D. Lb, Jojo, Ac, Luiz, Nd, and Nampoothiri, Se, “Sirenomelia: Case reports and current concepts of pathogenesis”, Pediatric and Developmental Pathology, vol. 15, pp. 403-406, 2016.

Publisher : Pediatric and Developmental Pathology

Year : 2016

Reciprocal Microduplication of the Williams-Beuren Syndrome Chromosome Region in a 9-Year-Old Omani Boy.

Cite this Research Publication : S. Mohan, Nampoothiri, S., Yesodharan, D., Venkatesan, V., Koshy, T., Paul, S. F. D., and Perumal, V., “Reciprocal Microduplication of the Williams-Beuren Syndrome Chromosome Region in a 9-Year-Old Omani Boy.”, Lab Med, vol. 47, no. 2, pp. 171-5, 2016.

Publisher : Lab Med

Areas of Interest
  • Children with dysmorphism and development delay
  • Prenatal testing and counselling for couple with family history of genetic disorders.
Qualifications
  • 2003 – MBBS from Govt. Medical College, Kottayam
  • 2009 – MD Paediatrics from Kasturba Medical College, Manipal
Work Experience
  • 2016 – present

    Working as Associate Professor of Paediatrics in the Division of Paediatric Genetics

  • 2010-2016

    Joined Amrita Hospital, Kochi as Assistant Professor of Paediatrics in the Division of Paediatric Genetics

  • 2009-2010

    Tutor in Paediatric Hematology-Oncology, Christian Medical College, Vellore

Presentations
  • Hemolytic Uremic Syndrome(HUS) mutation provenA Retrospective Diagnosis (First prize for poster-Amrita Hematocon 2014)
  • Williams – Beuren syndrome: Phenotypic variation from 3 months to 38 years and cardiac spectrum
    A 7.5 year experience from a Tertiary care centre in Kerala.(Second prize for poster in Kerala Pedicon-2013)
  • Oral free paper presentation- Clinical and Cardiologic spectrum in Di George Syndrome
    A series of 125 patients from a tertiary care centre over 8 years.
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