| Revision as of 01:37, 12 December 2008 editLegobot (talk | contribs)Bots1,667,985 editsm Robot - Moving category Diseases to Diseases and disorders per CFD at Misplaced Pages:Categories for discussion/Log/2008 December 2.← Previous edit | Revision as of 18:11, 14 December 2008 edit undoCitation bot (talk | contribs)Bots5,408,026 editsm Citation maintenance. Added: doi. You can use this bot yourself! Please report any bugs.Next edit → | ||
| Line 13: | Line 13: | ||
| MeshID = D006014 | | MeshID = D006014 | | ||
| }} | }} | ||
| '''Phosphofructokinase deficiency''', also known as '''Glycogen storage disease type VII''' or '''Tarui's disease''',<ref>{{WhoNamedIt|synd|3022}}</ref><ref name="pmid14339001">{{cite journal |author=Tarui S, OKuno G, Ikura Y, Tanaka T, Suda M, Nishikawa M |title=Phosphofructokinase Deficiency In Skeletal Muscle. A New Type Of Glycogenosis |journal=Biochem. Biophys. Res. Commun. |volume=19 |issue= |pages=517–23 |year=1965 |pmid=14339001 |doi= |url=}}</ref> is ] with ] inheritance. | '''Phosphofructokinase deficiency''', also known as '''Glycogen storage disease type VII''' or '''Tarui's disease''',<ref>{{WhoNamedIt|synd|3022}}</ref><ref name="pmid14339001">{{cite journal |author=Tarui S, OKuno G, Ikura Y, Tanaka T, Suda M, Nishikawa M |title=Phosphofructokinase Deficiency In Skeletal Muscle. A New Type Of Glycogenosis |journal=Biochem. Biophys. Res. Commun. |volume=19 |issue= |pages=517–23 |year=1965 |pmid=14339001 |doi= 10.1016/0006-291X(65)90156-7|url=}}</ref> is ] with ] inheritance. | ||
| It may affect humans as well as other ]s (especially ]s).<ref name="pmid8702726">{{cite journal |pmid=8702726 |url=http://www.jbc.org/cgi/pmidlookup?view=long&pmid=8702726 |doi=10.1074/jbc.271.33.20070 |title=Molecular Basis of Canine Muscle Type Phosphofructokinase Deficiency |year=1996 |author=Stedman, H. |journal=Journal of Biological Chemistry |volume=271 |pages=20070}}</ref> In humans it is the least common type of ]. | It may affect humans as well as other ]s (especially ]s).<ref name="pmid8702726">{{cite journal |pmid=8702726 |url=http://www.jbc.org/cgi/pmidlookup?view=long&pmid=8702726 |doi=10.1074/jbc.271.33.20070 |title=Molecular Basis of Canine Muscle Type Phosphofructokinase Deficiency |year=1996 |author=Stedman, H. |journal=Journal of Biological Chemistry |volume=271 |pages=20070}}</ref> In humans it is the least common type of ]. | ||
| Line 20: | Line 20: | ||
| In this condition, a deficiency of the M subunit of the ] ] impairs the ability of cells such as ] and ]s to use ]s (such as ]) for energy. | In this condition, a deficiency of the M subunit of the ] ] impairs the ability of cells such as ] and ]s to use ]s (such as ]) for energy. | ||
| Unlike most other glycogen storage diseases, it directly affects ].<ref name="pmid11949936">{{cite journal |author=Nakajima H, Raben N, Hamaguchi T, Yamasaki T |title=Phosphofructokinase deficiency; past, present and future |journal=Curr. Mol. Med. |volume=2 |issue=2 |pages=197–212 |year=2002 |pmid=11949936 |doi= |url=http://www.bentham-direct.org/pages/content.php?CMM/2002/00000002/00000002/0009M.SGM}}</ref> | Unlike most other glycogen storage diseases, it directly affects ].<ref name="pmid11949936">{{cite journal |author=Nakajima H, Raben N, Hamaguchi T, Yamasaki T |title=Phosphofructokinase deficiency; past, present and future |journal=Curr. Mol. Med. |volume=2 |issue=2 |pages=197–212 |year=2002 |pmid=11949936 |doi= 10.2174/1566524024605734|url=http://www.bentham-direct.org/pages/content.php?CMM/2002/00000002/00000002/0009M.SGM}}</ref> | ||
| ==Presentation== | ==Presentation== | ||
Revision as of 18:11, 14 December 2008
Medical condition| Phosphofructokinase deficiency | |
|---|---|
| Specialty | Endocrinology  |
Phosphofructokinase deficiency, also known as Glycogen storage disease type VII or Tarui's disease, is metabolic disorder with autosomal recessive inheritance.
It may affect humans as well as other mammals (especially dogs). In humans it is the least common type of glycogen storage disease.
Pathophysiology
In this condition, a deficiency of the M subunit of the phosphofructokinase enzyme impairs the ability of cells such as erythrocytes and rhabdomyocytes to use carbohydrates (such as glucose) for energy.
Unlike most other glycogen storage diseases, it directly affects glycolysis.
Presentation
The disease presents with exercise-induced muscle cramps and weakness (sometimes rhabdomyolysis), as well as with haemolytic anaemia causing dark urine a few hours later.
See also
References
- synd/3022 at Who Named It?
- Tarui S, OKuno G, Ikura Y, Tanaka T, Suda M, Nishikawa M (1965). "Phosphofructokinase Deficiency In Skeletal Muscle. A New Type Of Glycogenosis". Biochem. Biophys. Res. Commun. 19: 517–23. doi:10.1016/0006-291X(65)90156-7. PMID 14339001.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - Stedman, H. (1996). "Molecular Basis of Canine Muscle Type Phosphofructokinase Deficiency". Journal of Biological Chemistry. 271: 20070. doi:10.1074/jbc.271.33.20070. PMID 8702726.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - Nakajima H, Raben N, Hamaguchi T, Yamasaki T (2002). "Phosphofructokinase deficiency; past, present and future". Curr. Mol. Med. 2 (2): 197–212. doi:10.2174/1566524024605734. PMID 11949936.
{{cite journal}}: CS1 maint: multiple names: authors list (link)
External links
- Glycogen storage disease type 7; Muscle phosphofructokinase deficiency; Tarui disease at NIH's Office of Rare Diseases
 | This genetic disorder article is a stub. You can help Misplaced Pages by expanding it. |