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pro vyhledávání: '"Susanta Sadhukhan, MSc"'
Autor:
Ajitesh Roy, MD, DM, Rana Bhattacharjee, MD, DM, MRCP, Soumik Goswami, MD, DM, Partha P. Chakraborty, MD, DNB, DM, S. Chitra, MD, DM, Anubhab Thukral, MD, DM, Susanta Sadhukhan, MSc, Biswabandhu Bankura, MSc, Madhusudan Das, PhD, Kousik Biswas, MD, DM, Subhankar Chowdhury, MD, DM, MRCP
Publikováno v:
AACE Clinical Case Reports, Vol 3, Iss 4, Pp 322-325 (2017)
ABSTRACT: Objective: 17-α-Hydroxylase deficiency (17-OHD) is a very rare disorder of adrenal and gonadal steroidogeneis. The patient usually presents as a phenotypic female with hypertension, hypokalemia, and delayed puberty due to hypergonadotropic
Externí odkaz:
https://doaj.org/article/368229af0c7a4a689896d97c5edf1022
