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Pediatr Diabetes ; 18(5): 327-331, 2017 08.
Article in English | MEDLINE | ID: mdl-28568353

ABSTRACT

Prior to 1971, type Ia glycogen storage disease was marked by life-threatening hypoglycemia, lactic acidosis, severe failure to thrive, and developmental delay. With the introduction of continuous feeds in the 1970s and cornstarch in the 1980s, the prognosis improved, but complications almost universally developed. Changes in the management of type Ia glycogen storage disease have resulted in improved metabolic control, and this manuscript reviews the increasing evidence that complications can be delayed or prevented with optimal metabolic control as previously was seen in diabetes.


Subject(s)
Glycogen Storage Disease Type I/therapy , Precision Medicine , Renal Insufficiency/prevention & control , Adenoma/complications , Adenoma/prevention & control , Adult , Child , Combined Modality Therapy , Glycogen Storage Disease Type I/blood , Glycogen Storage Disease Type I/complications , Glycogen Storage Disease Type I/diagnosis , Humans , Hypoglycemia/complications , Hypoglycemia/prevention & control , Liver Neoplasms/complications , Liver Neoplasms/prevention & control , Nephrocalcinosis/complications , Nephrocalcinosis/prevention & control , Nephrolithiasis/complications , Nephrolithiasis/prevention & control , Osteoporosis/complications , Osteoporosis/prevention & control , Prognosis , Renal Insufficiency/complications
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