17 alpha-hydroxylase deficiency natural history, complications and prognosis
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2], Mehrian Jafarizade, M.D [3]
Overview
Overview
If left untreated, patients with 17 alpha-hydroxylase deficiency may progress to develop malignant hypertension. Common complications of 17 alpha-hydroxylase deficiency include muscle weakness, metabolic alkalosis, and infertility. Prognosis is generally good with treatment.
Natural History
Natural History
If left untreated, patients with 17 alpha-hydroxylase deficiency may progress to develop malignant hypertension.
Complications
Complications
Complications of Hypertension
- Vascular hemorrhage
- Renal insufficiency
- Left ventricular hypertrophy
- Hypertensive retinopathy
- Stroke
Complications of Hypokalemia
Other Complications
Prognosis
Prognosis
- The prognosis of 17 alpha-hydroxylase deficiency is generally good or excellent.
References
References
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