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STEROID PANEL, 21- HYDROXYLASE DEFICIENCY/STRESS DIFERENTIATION

Steroid 21- hydroxylase deficiency accounts for more than 90% of the cases of Congenital Adrenal Hyperplasia (CAH). The classical form of CAH presents in childhood with markedly raised 17- hydroxypregesterone (17-OHP). Neonates are screened for CAH by testing 17-OHP levels to reduce mortality and other serious sequelae. False positive results can occur due to physiological stress. Steroid profiling by LCMS/MS improves the positive predictive value of newborn screening for Congenital Adrenal Hyperplasia (CAH).

Parameter(s) covered : 5
Report Frequency: Sample Mon / Thu by 9 am; Report Wed / Sat
Special Instruction: Diurnal variation present; sample will be taken between 8-10 am OR 4-6 pm.

Price : ₹ 2700.00

Parameters

  1. 17-Hydroxyprogesterone (17-OHP)
  2. 17-OHP + 21-deoxycortisol : Cortisol Ratio
  3. 21-deoxycortisol
  4. Androstenedione
  5. Cortisol