55:
1136:
29:
110:. For those diagnosed with essential pentosuria, the major isozyme appears to be the same as the minor one. Alimentary pentosuria can be acquired through fruits high in pentose. Finally, drug-induced pentosuria can be developed by those exposed to morphine, fevers, allergies, and some hormones.
99:. Patients of pentosuria have a low concentration of the sugar d-xyloketose. Using phenyl pentosazone crystals, phloroglucin reaction, and absorption spectrum, pentose can be traced back as the reducing substance in urine, with those that have pentosuria.
519:
504:
595:
1197:
102:
Research has shown that pentosuria appears in 3 forms. The most widely studied is essential pentosuria, where a couple of grams of L-xylusol are released into a person's system daily.
588:
160:
Scriver CR (October 2008). "Garrod's
Croonian Lectures (1908) and the charter 'Inborn Errors of Metabolism': albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008".
782:
95:, so it may give false diagnosis of diabetes, as it is found in high concentrations in urine. However glucose metabolism is normal in people with pentosuria, and they are not
1202:
581:
573:
1173:
1060:
1076:
677:
608:
80:
214:
1166:
987:
358:
B.Tower, Donald; Edmund L. Peters; Milton A. Pogorelskin (January 1956). "Nature and
Significance of Pentosuria in Neuromuscular Disease".
534:
1032:
876:
926:
894:
882:
831:
1159:
1037:
1027:
888:
837:
825:
752:
672:
981:
786:
113:
Those diagnosed with
Pentosuria are predominantly of Jewish root. However, it is a harmless defect, and no cure is needed.
976:
1110:
992:
604:
1052:
916:
1065:
777:
618:
545:
698:
687:
1097:
997:
747:
404:
Lane, A.B. (February 1984). "On the Nature of L-Xylulose
Reductase Deficiency in Essential Pentosuria".
103:
84:
54:
653:
648:
523:
204:
900:
848:
429:
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335:
185:
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43:
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250:
169:
1019:
203:
Julia A. McMillan; Ralph D. Feigin; Catherine DeAngelis; M. Douglas Jones (1 April 2006).
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843:
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612:
255:
238:
92:
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48:
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173:
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471:
379:
264:
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425:
331:
912:
808:
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96:
88:
36:
1142:
This article about an endocrine, nutritional, or metabolic disease is a
496:
951:
804:
717:
627:
417:
371:
107:
72:
68:
353:
351:
349:
106:, contained in red blood cells, is composed of both a major and minor
1114:
972:
713:
508:
315:
239:"Sir Archibald Garrod's "Inborn Errors of Metabolism" IV.Pentosuria"
28:
76:
1008:
539:
577:
929:(Pompe's disease, glucosidase deficiency, formerly GSD-IIa)
79:
in unusually high concentrations. It was characterized as
1040:(von Gierke's disease, glucose 6-phosphatase deficiency)
885:(Hers' disease, liver glycogen phosphorylase deficiency)
1147:
280:"The Nature of the Sugar in Four Cases of Pentosuria"
1109:
Fatal congenital nonlysosomal cardiac glycogenosis (
486:
1085:
1051:
1018:
963:
950:
910:
867:
858:
816:
803:
761:
735:
725:
712:
662:
638:
626:
490:
42:
21:
1198:Endocrine, nutritional and metabolic disease stubs
209:. Lippincott Williams & Wilkins. pp. 1–.
984:(Tarui's disease, phosphofructokinase deficiency)
834:(Andersen's disease, branching enzyme deficiency)
450:(May 1959). "Pentose Metabolism and Pentosuria".
891:(McArdle's disease, myophosphorylase deficiency)
879:(Cori's disease, debranching enzyme deficiency)
399:
397:
83:in 1908. It is associated with a deficiency of
1167:
589:
8:
1061:Glucose-6-phosphate dehydrogenase deficiency
206:Oski's pediatrics: principles & practice
130:
128:
126:
1077:6-phosphogluconate dehydrogenase deficiency
1174:
1160:
960:
864:
813:
732:
722:
635:
596:
582:
574:
487:
81:an inborn error of carbohydrate metabolism
53:
27:
18:
1009:Mitochondrial pyruvate carrier deficiency
298:
254:
1203:Inborn errors of carbohydrate metabolism
678:Inborn errors of renal tubular transport
122:
87:, necessary for xylitol metabolism. L-
243:The American Journal of Human Genetics
7:
1132:
1130:
988:Triosephosphate isomerase deficiency
935:(LAMP2 deficiency, formerly GSD-IIb)
1002:Phosphoglucose isomerase deficiency
903:(PGM1-CDG, CDG1T, formerly GSD-XIV)
287:The Journal of Biological Chemistry
1146:. You can help Knowledge (XXG) by
1033:Fructose bisphosphatase deficiency
1005:Phosphoglycerate kinase deficiency
14:
897:(phosphorylase kinase deficiency)
320:Experimental Biology and Medicine
278:Greenwald, Isidor (17 May 1930).
237:Knox, W. Eugene (December 1958).
1134:
927:Glycogen storage disease type II
452:The American Journal of Medicine
1028:Pyruvate carboxylase deficiency
838:Adult polyglucosan body disease
673:Glucose-galactose malabsorption
67:is a condition where the sugar
828:(glycogen synthase deficiency)
1:
901:Phosphoglucomutase deficiency
300:10.1016/S0021-9258(18)76792-6
1111:AMP-activated protein kinase
464:10.1016/0002-9343(59)90231-1
1219:
1129:
1073:(Transketolase deficiency)
993:Pyruvate kinase deficiency
314:Stookey, LB (1 May 1909).
1053:Pentose phosphate pathway
619:glycogen storage diseases
174:10.1007/s10545-008-0984-9
35:
26:
1066:Transaldolase deficiency
551:C536652 C536652, C536652
851:(glycogenin deficiency)
699:Fanconi-Bickel syndrome
609:carbohydrate metabolism
140:Encyclopædia Britannica
688:Fructose malabsorption
162:J. Inherit. Metab. Dis
1098:Primary hyperoxaluria
998:Aldolase A deficiency
748:Essential fructosuria
615:metabolism disorders
332:10.3181/00379727-6-72
753:Fructose intolerance
649:Congenital alactasia
406:Biochemical Genetics
104:L-xylulose reductase
85:L-xylulose reductase
654:Sucrose intolerance
701:(GLUT2 deficiency)
695:(GLUT1 deficiency)
418:10.1007/bf00499113
372:10.1212/wnl.6.1.37
75:, presents in the
1155:
1154:
1124:
1123:
1047:
1046:
1011:(MPC1 deficiency)
946:
945:
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798:
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794:
708:
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571:
570:
216:978-0-7817-3894-1
62:
61:
16:Medical condition
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733:
723:
682:Renal glycosuria
636:
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1125:
1120:
1081:
1043:
1020:Gluconeogenesis
1014:
938:
911:
906:
869:Extralysosomal:
868:
854:
791:
787:GALE deficiency
783:GALT deficiency
778:GALK deficiency
762:
757:
736:
704:
693:De Vivo Disease
658:
632:(extracellular)
631:
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862:
860:Glycogenolysis
856:
855:
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846:
844:Lafora disease
841:
835:
829:
822:
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811:
801:
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797:
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790:
789:
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727:Monosaccharide
720:
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690:
685:
675:
669:
667:
664:Monosaccharide
660:
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651:
645:
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633:
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623:
613:monosaccharide
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491:Classification
484:
483:External links
481:
478:
477:
448:Touster, Oscar
439:
412:(1–2): 61–72.
393:
366:(137): 37–49.
345:
326:(5): 135–136.
306:
270:
229:
215:
195:
152:
121:
120:
118:
115:
93:reducing sugar
60:
59:
46:
40:
39:
33:
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24:
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10:
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4:
3:
2:
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1133:
1128:
1116:
1112:
1108:
1106:
1103:
1099:
1096:
1095:
1094:
1093:Hyperoxaluria
1091:
1090:
1088:
1084:
1078:
1075:
1072:
1069:
1067:
1064:
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1059:
1058:
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1023:
1021:
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1001:
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994:
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989:
986:
983:
980:
978:
974:
971:
970:
968:
966:
962:
959:
957:
953:
949:
934:
933:Danon disease
931:
928:
925:
924:
922:
918:
914:
909:
902:
899:
896:
893:
890:
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839:
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629:
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579:
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541:
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515:
511:
510:
506:
502:
501:
498:
493:
489:
482:
473:
469:
465:
461:
458:(5): 724–39.
457:
453:
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431:
427:
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419:
415:
411:
407:
400:
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317:
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296:
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271:
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257:
252:
249:(4): 385–97.
248:
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233:
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183:
179:
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168:(5): 580–98.
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109:
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56:
50:
49:Endocrinology
47:
45:
41:
38:
34:
30:
25:
20:
1148:expanding it
1141:
1126:
1113:deficiency,
1104:
982:GSD type VII
877:GSD type III
818:Glycogenesis
768:galactosemia
640:Disaccharide
605:Inborn error
555:
544:
533:
518:
503:
455:
451:
442:
409:
405:
363:
359:
323:
319:
316:"Pentosuria"
309:
290:
286:
273:
246:
242:
232:
220:. Retrieved
205:
198:
165:
161:
155:
143:. Retrieved
139:
136:"pentosuria"
112:
101:
64:
63:
895:GSD type IX
883:GSD type VI
849:GSD type XV
832:GSD type IV
630:, transport
1187:Categories
1105:Pentosuria
1038:GSD type I
965:Glycolysis
889:GSD type V
826:GSD type 0
729:catabolism
642:catabolism
617:Including
557:DiseasesDB
117:References
65:Pentosuria
22:Pentosuria
913:Lysosomal
764:Galactose
666:transport
360:Neurology
340:209361414
222:5 January
145:March 26,
44:Specialty
809:glycogen
738:Fructose
472:13649698
434:23655195
388:24664586
380:13280026
265:13606116
190:10154482
182:18850300
97:diabetic
89:Xylulose
37:Xylulose
952:Glucose
805:Glucose
718:glucose
628:Sucrose
426:3994659
293:: 1,2.
256:1931884
108:isozyme
73:pentose
69:xylitol
1115:PRKAG2
973:MODY 2
840:(APBD)
714:Hexose
540:260800
470:
432:
424:
386:
378:
338:
263:
253:
213:
188:
180:
51:
1193:Urine
1086:Other
1071:SDDHD
621:(GSD)
529:271.8
514:E74.8
430:S2CID
384:S2CID
336:S2CID
283:(PDF)
186:S2CID
91:is a
77:urine
1144:stub
977:HHF3
562:9816
546:MeSH
535:OMIM
524:9-CM
468:PMID
422:PMID
376:PMID
261:PMID
224:2011
211:ISBN
178:PMID
147:2013
71:, a
956:CAC
917:LSD
607:of
520:ICD
505:ICD
460:doi
414:doi
368:doi
328:doi
295:doi
251:PMC
170:doi
1189::
954:⇄
919:):
807:⇄
766:/
716:→
611::
560::
549::
538::
527::
512::
509:10
466:.
456:26
454:.
428:.
420:.
410:23
408:.
396:^
382:.
374:.
362:.
348:^
334:.
322:.
318:.
291:88
289:.
285:.
259:.
247:10
245:.
241:.
184:.
176:.
166:31
164:.
138:.
125:^
1175:e
1168:t
1161:v
1150:.
1117:)
975:/
915:(
785:/
770::
740::
684:)
680:(
597:e
590:t
583:v
522:-
507:-
497:D
474:.
462::
436:.
416::
390:.
370::
364:6
342:.
330::
324:6
303:.
297::
267:.
226:.
192:.
172::
149:.
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
