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Fructosuria

Fructosuria is an autosomal recessive disorder caused by mutations of the KHK gene. It is characterized by intermittent renal excretion of fructose.

Systematic

Monosacchariduria
Fructosuria
KHK
Glucose-Galactose Malabsorption
Renal Glucosuria

References:

1.

Albanese C et al. (1996) The gonadotropin genes: evolution of distinct mechanisms for hormonal control.

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2.

Raivio T et al. (1996) The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys.

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3.

Muyan M et al. (1996) The carboxy-terminal region of the beta-subunits of luteinizing hormone and chorionic gonadotropin differentially influence secretion and assembly of the heterodimers.

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4.

van den Heuvel LP et al. (2002) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).

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5.

MONASTERIO G et al. (1964) RENAL DIABETES AS A CONGENITAL TUBULAR DYSPLASIA.

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6.

Elsas LJ et al. (1971) Autosomal recessive inheritance of renal glycosuria.

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7.

OMIM.ORG article

Omim 606824 external link
8.

Wikipedia article

Wikipedia EN (Glucose-galactose_malabsorption) external link
Update: Aug. 14, 2020
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