Phosphofructokinase deficiency
- Phosphofructokinase deficiency
Infobox_Disease
Name = PAGENAME
Caption =
DiseasesDB = 5314
ICD10 = ICD10|E|74|0|e|70
ICD9 = ICD9|271.0
ICDO =
OMIM = 232800
MedlinePlus =
eMedicineSubj = med
eMedicineTopic = 913
MeshID = D006014
Phosphofructokinase deficiency, also known as Glycogen storage disease type VII or Tarui's disease, [WhoNamedIt|synd|3022] [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=] is metabolic disorder with autosomal recessive inheritance.]It may affect humans as well as other mammals (especially dogs).[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] 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.[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] ]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.
ee also
* PFKM
* Seiichiro Tarui
References
External Links
*RareDiseases|5686|Glycogen storage disease type 7; Muscle phosphofructokinase deficiency; Tarui disease
Wikimedia Foundation.
2010.
Look at other dictionaries:
Phosphofructokinase — PFK redirects here. PFK (Poulet Frit Kentucky) is also the name for KFC in French speaking Quebec, Canada. For the Polish hip hop group, see Paktofonika. Phosphofructokinase Identifiers Symbol Ppfruckinase Pfam … Wikipedia
muscle phosphofructokinase deficiency — mus·cle phos·pho·fruc·to·ki·nase de·fi·cien·cy (musґəl fos″fo frook″to kiґnās) glycogen storage disease, type VII … Medical dictionary
6-phosphofructokinase — Phosphofructokinase I; an enzyme that catalyzes the phosphorylation of d fructose 6 phosphate by ATP (or other NTP) to fructose 1,6 bisphosphate and ADP (or other NDP); this enzyme catalyzes a step in glycolysis; it is inhibited by elevated… … Medical dictionary
Pyruvate carboxylase deficiency — Classification and external resources Oxaloacetate is the product of pyruvate carboxylase ICD 10 E … Wikipedia
Galactose-1-phosphate uridylyltransferase deficiency — Classification and external resources Galactose ICD 10 E … Wikipedia
1-phosphofructokinase — Fructose 1 phosphate kinase; an enzyme catalyzing phosphorylation of d fructose 1 phosphate by ATP (or other NTP) to d fructose 1,6 bisphosphate and ADP (or other NDP); a key step in the metabolism of d fructose; a deficiency of the muscle enzyme … Medical dictionary
PFKM — Phosphofructokinase, muscle, also known as PFKM, is a human gene.cite web | title = Entrez Gene: PFKM phosphofructokinase, muscle| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5213| accessdate = ] PBB… … Wikipedia
PFKL — Phosphofructokinase, liver, also known as PFKL, is a human gene.cite web | title = Entrez Gene: PFKL phosphofructokinase, liver| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5211| accessdate = ] PBB… … Wikipedia
Rhabdomyolysis — Classification and external resources Urine from a person with rhabdomyolysis showing the characteristic brown discoloration as a result of myoglobinuria … Wikipedia
glycogenosis — Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the … Medical dictionary