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12-lead e. that performed using the twelve standard leads: the three standard bipolar limb leads, the three augmented unipolar limb leads (aVF, aVL, and aVR), and the six standard precordial leads (V1 to V6).
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15-l. arachidonate 15-lipoxygenase.
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17α-h. steroid 17α-monooxygenase.
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17α-hydroxylase deficiency an autosomal recessive disorder of steroidogenesis in which deficiency of steroid 17α-monooxygenase causes one type of congenital adrenal hyperplasia (type V). The disorder is characterized by decreased cortisol, androgens, estrogens, and aldosterone production and increases in 17-deoxysteroids such as corticosterone and deoxycorticosterone, resulting in hypertension, hypokalemia, and hypogonadism. Severe deficiency during fetal life can cause male pseudohermaphroditism; postnatally, it can impair sexual development in both males and females. See table at hyperplasia and see also 17,20 lyase deficiency.
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17α-hydroxyprogesterone an intermediate formed in the conversion of cholesterol to cortisol, androgens, and estrogens.
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