1.Diabetes and COVID-19: A review
Arjun Baidya ; Santosh Kumar Singh ; Sarita Bajaj ; Abdul Hamid Zargar ; Parminder Singh ; Sambit Das ; Anand Shankar
Journal of the ASEAN Federation of Endocrine Societies 2020;35(1):40-48
Coronavirus Disease 2019 (COVID-19) is an emerging disease and since its first identification in Wuhan, China, in December 2019, there has been a rapid increase in cases and deaths across the world. COVID-19 has been shown to have an immense impact in infected persons with diabetes, worsening their outcome, especially in elderly, smokers, obese, those having CVD, CKD, poor glycemic control and long duration of diabetes. In this review we summarize the current understanding of `the impact of COVID-19 on diabetes and discusses the pathophysiological mechanisms and management of diabetes and its complication in this scenario.
COVID-19
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Diabetes Mellitus
2.Laron syndrome: A tale of two siblings
Niladri Das ; Silima Subhasnigdha Tarenia ; Souvik Saha ; Prashant Manohar Gaikwad ; Deep Kamlesh Hathi ; Soumik Goswami ; Arjun Baidya ; Nilanjan Sengupta
Journal of the ASEAN Federation of Endocrine Societies 2023;38(2):124-127
Primary growth hormone (GH) resistance or growth hormone insensitivity syndrome, also called Laron syndrome, is a hereditary disease caused by mutations in the GH receptor or in the post-receptor signaling pathway. This disorder is characterized by postnatal growth failure resembling GH deficiency. Differentiating the two conditions is necessary. We present the cases of two siblings, a 16-year-old female and a 9-year-old male, born from a consanguineous union. Both had normal birth weights with subsequent severe short stature and delayed teeth eruption, with no features suggestive of any systemic illness. Serum insulin-like growth factor 1 (IGF1) and insulin-like growth factor binding protein 3 (IGFBP3) were both low. Suspecting GH deficiency, provocative testing with clonidine was done revealing peak growth hormone >40 ng/mL in both patients. In view of low IGF1 and IGFBP3 and high GH on stimulation, IGF1 generation test was done for both siblings, with values supporting the diagnosis of GH insensitivity or Laron syndrome.
Laron Syndrome
3.Swyer syndrome presenting as dysgerminoma: A case report
Silima Tarenia ; Sujaya Chattopadhyay ; Niladri Das ; Deep Hathi ; Arjun Baidya ; Puranjoy Chakrabarty ; Nilanjan Sengupta ; Soumik Goswami
Journal of the ASEAN Federation of Endocrine Societies 2023;38(1):108-113
Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but typical Mullerian structures in a phenotypically female individual. The condition presents as primary amenorrhoea or delayed puberty. Eventually, malignant neoplasms may arise. We report a case of a 16-year-old patient with Swyer syndrome presenting with primary amenorrhoea and with previous diagnosis four years earlier of a malignant dysgerminoma in the right ovary.
Swyer syndrome
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dysgerminoma
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gonadal dysgenesis