Boyd-Stearns syndrome: Difference between revisions
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==Overview== | ==Overview== | ||
Boyd-Stearns syndrome is characterized by | 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== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Nephrology]] | [[Category:Nephrology]] | ||
[[Category:Grammar]] | [[Category:Grammar]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
Revision as of 23:52, 22 July 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