Boyd-Stearns syndrome

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Raviteja Guddeti, M.B.B.S.[3]

Overview

Boyd-Stearns syndrome is characterized by glycosuria, acidosis, albuminuria and hypochloremia.

Symptoms include rickets during infancy, short stature, low blood phosphate levels, malnutrition and osteoporosis.