ba0004p74 | (1) | ICCBH2015
Awogbemi Olumoyin
, Safdar Asimah
, McEnaney Rachel
, Mahmood Nasim
, Donne Adam
, Weber Astrid
, Dharmaraj Poonam
Background: Hypophosphataemic rickets (HPR) is an inherited condition of phosphate wasting associated with abnormal bone biochemistry and features of rickets. Most patients respond to treatment with alfacalcidol and oral phosphate. Raised levels of alkaline phosphatase (ALP) and parathyroid hormone (PTH) generally indicate a need for refining treatment, or poor compliance.Presenting problem: We report the case of a 36 week gestation male infant born to c...