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Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: Report of three new mutations

Bachrach, BE (author)
Weinstein, DA (author)
Orho-Melander, Marju (author)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Diabetes - kardiovaskulär sjukdom,Genomics, Diabetes and Endocrinology,Lund University Research Groups,Diabetes - Cardiovascular Disease
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Burgess, A (author)
Wolfsdorf, JI (author)
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 (creator_code:org_t)
Elsevier BV, 2002
2002
English.
In: Journal of Pediatrics. - : Elsevier BV. - 1097-6833 .- 0022-3476. ; 140:6, s. 781-783
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Although glycogen storage disease type 0 (GSD0) is included in the differential diagnosis of ketotic hypoglycemia, it usually is not considered in the evaluation of glucosuria or hyperglycemia. We describe two children with GSD0, confirmed by mutation analysis, who had glucosuria and hyperglycemia. Because of the variable presentation of this disorder and previous dependence on liver biopsy to confirm diagnosis, it is likely that GSD0 is underdiagnosed.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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Bachrach, BE
Weinstein, DA
Orho-Melander, M ...
Burgess, A
Wolfsdorf, JI
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
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and Endocrinology an ...
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