Boyd-Stearns syndrome
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief:Raviteja Guddeti, M.B.B.S.[2]
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.
References