Boyd-Stearns syndrome: Difference between revisions
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{{CMG}}; '''Associate Editor(s)-In-Chief:'''[[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto:rgudetti@perfuse.org] | {{CMG}}; '''Associate Editor(s)-In-Chief:'''[[User: Raviteja Reddy Guddeti| Raviteja Guddeti, M.B.B.S.]][mailto:rgudetti@perfuse.org] | ||
==Overview== | ==Overview== | ||
Revision as of 15:58, 7 August 2012
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.
Diagnosis
Symptoms
- Rickets during infancy
- Short stature
- Low blood phosphate levels
- Malnutrition
- Osteoporosis
References