Journal of Genetic Disorders

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Relevant Topics
  • Achondroplasia
  • Chromosomal Aberrations
  • Cystic fibrosis (CF)
  • DNA Depurination
  • Down syndrome (DS or DNS)
  • Duchenne muscular dystrophy (DMD)
  • Fragile X syndrome (FXS)
  • Haemophilia
  • Huntington′s disease (HD)
  • Jackson-Weiss Syndrome
  • Maple syrup urine disease (MSUD)
  • Marfan syndrome
  • Neurofibromatosis
  • Pachyonychia Congenita (PC)
  • Phenylketonuria
  • Severe Combined Immunodeficiency (SCID)
  • Sickle cell anemia
  • Smith-Lemli-Opitz syndrome (SLOS)
  • Thalassemia
  • Turner syndrome
  • WAGR syndrome
  • Williams syndrome

Dr. Meghmala Sadhukhan

Dr. Meghmala Sadhukhan
Department of Pediatrics, Tunbridge Wells Hospital Royal, Tunbridge Wells, UK

Biography

Dr. Meghmala Sadhukhan had completed DCH from Kolkata and MRCPCH from UK. She was working in UK for 5years in Paediatrics and gained experience in General Paediatrics, Neonatology and Paediatric Gastroenterology with experience in paediatric GI endoscopy. Her research interests include genetic conditions related to Paediatric Gastroenterology.