A Rare Case of Turner’s Syndrome with Deaf-mutism Reporting at Government Medical College, Patiala, Punjab, India

Authors

  • Harshindar Kaur Associate Professor, Department of Pediatrics, GMC Patiala, Punjab, India,
  • anjana Saholi Junior Resident , PCMS, Patiala, Punjab, India,
  • Pehal Goyal Senior Resident, Patiala, Punjab, India,
  • Kulwant Rai Junior Resident , PCMS, Patiala, Punjab, India

Keywords:

Turner’s syndrome, ovarian failure, lymphedema, deaf-mutism

Abstract

Abstract :Turner syndrome (TS), also known as Congenital ovarian hypoplasia syndrome, is a neurogenetic disorder characterized by partial or complete monosomy-X. Despite an often conspicuous phenotype, the diagnostic delay can be substantial and the average age at diagnosis is around 15 years of age. Morbidity and mortality are increased in women with Turner syndrome compared with the general population and the involvement of multiple organs through all stages of life necessitates a multidisciplinary approach to care. Treatment may include growth hormone therapy at appropriate time for short stature and estrogen therapy to help stimulate sexual development.

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Published

31-12-2021

How to Cite

Harshindar Kaur, anjana Saholi, Pehal Goyal, & Kulwant Rai. (2021). A Rare Case of Turner’s Syndrome with Deaf-mutism Reporting at Government Medical College, Patiala, Punjab, India. GMC Patiala Journal of Research and Medical Education, 4(2), 49–51. Retrieved from https://jrme.gmcpatiala.edu.in/index.php/j/article/view/89

Issue

Section

Case Report