Now showing items 1-2 of 2

    • 21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency 

      Tonetto-Fernandes, Vânia [UNIFESP]; Lemos-Marini, Sofia Helena Valente de; Mello, Maricilda Palandi de; Ribeiro-Neto, Luciane Maria [UNIFESP]; Kater, Claudio Elias [UNIFESP] (Walter De Gruyter Gmbh, 2008-05-01)
      21-Hydroxylase deficiency (21OHD) is the commonest form of congenital adrenal hyperplasia, while 11 beta OHD represents 5% of cases. Although both result from mutations in distinct genes, cases of 'apparent' combined 210HD ...

    • Adrenal steroids synthesis during acute infectious diseases in infants 

      Longui, C. A.; Zlochevsky, ERM; Bachega, Tania Aparecida Sartori Sanchez [UNIFESP]; Monte, O. (Freund Publishing House Ltd, 2002-11-01)
      An increase in plasma 17OHP found in infants requiring differential diagnosis between septic shock and adrenal failure led us to look for adrenal steroids pattern during infection. Infants and Methods: 56 infants, 1-6 ...