Sandbox/01: Difference between revisions

Jump to navigation Jump to search
← Older editNewer edit →
VisualWikitext
Donald Szlosek (talk | contribs)
nocaptcha
200 edits
No edit summary
Donald Szlosek (talk | contribs)
nocaptcha
200 edits
No edit summary
Line 1: Line 1:
{{Refimprove|date=August 2008}}
__NOTOC__
{{Infobox disease |
{{CMG}}
  Name          = Propionic acidemia |
  ICD10          = {{ICD10|E|71|1|e|70}} |
  ICD9          = {{ICD9|270.3}} |
  ICDO          = |
  Image          = Propionic acid structure.png  |
  Caption        = [[Propionic acid]] |
  OMIM          = 606054 |
  MedlinePlus    = |
  eMedicineSubj  = ped |
  eMedicineTopic = 1906 |
  DiseasesDB    = 29673 |
  DiseasesDB_mult = {{DiseasesDB2|29904}} |
}}


'''Propionic acidemia''', also known as '''propionic aciduria''', '''propionyl-CoA carboxylase deficiency''' and '''ketotic glycinemia''',<ref>{{OMIM|606054}}</ref> is an [[autosomal]] [[recessive]]<ref>{{cite journal |pmid=10820128 |date=July 2000 |author1=Ravn K |author2=Chloupkova M |author3= Christensen E |author4=Brandt NJ |author5=Simonsen H |author6=Kraus JP |author7=Nielsen IM |author8=Skovby F |author9=Schwartz M |title=High incidence of propionic acidemia in greenland is due to a prevalent mutation, 1540insCCC, in the gene for the beta-subunit of propionyl CoA carboxylase |volume=67 |issue=1 |pages=203–206 |pmc=1287078 |doi=10.1086/302971 |journal=American Journal of Human Genetics}}</ref> [[metabolic disorder]], classified as a [[branched-chain amino acid|branched-chain]] [[organic acidemia]].<ref name="oad">{{cite journal |vauthors =Deodato F, Boenzi S, Santorelli FM, Dionisi-Vici C |title=Methylmalonic and propionic aciduria |journal=[[Am J Med Genet C Semin Med Genet]] |volume=142 |issue=2 |pages=104–112 |year=2006 |pmid=16602092 |doi=10.1002/ajmg.c.30090 }}</ref>
{{Editor Help}}


The disorder presents in the early [[neonatal]] period with progressive [[encephalopathy]]. Death can occur quickly, due to secondary [[hyperammonemia]], infection, cardiomyopathy, or basal ganglial stroke.<ref name="pbg">{{cite journal |vauthors =Hamilton RL, Haas RH, Nyhan WC, Powell HC, Grafe MR |title=Neuropathology of propionic acidemia: a report of two patients with basal ganglia lesions |journal=Journal of Child Neurology |volume=10 |issue=1 |pages=25–30 |year=1995 |pmid=7769173 |doi=10.1177/088307389501000107 }}</ref>
==Overview==
{{Infobox_Disease
| Name          = Vitamin B6 deficiency
| Image          =  
| Caption        =  
| DiseasesDB    = 13923
| ICD10          = {{ICD10|E|53|1|e|50}}
| ICD9          = {{ICD9|266.1}}
| ICDO          =
| OMIM          =
| MedlinePlus    =
| eMedicineSubj  = med
| eMedicineTopic = 1977
| MeshID        = D026681
}}
{{SI}}
The classic clinical syndrome for '''Pyridoxine deficiency''' (or '''B6 deficiency''') is a seborrheic dermatitis-like eruption, atrophic glossitis with ulceration, angular cheilitis, conjunctivitis, intertrigo, and neurologic symptoms of somnolence, confusion, and neuropathy.<ref>Andrews' Diseases of the Skin, 10th Edition, Elsevier.</ref>


Propionic acidemia is a rare disorder that is inherited from both parents. Being autosomal recessive, neither parent shows symptoms, but both carry a defective gene responsible for this disease. It takes two faulty genes to cause PA, so there is a 1 in 4 chance for these parents to have a child with PA.
Vitamin B6 is a co-factor for glutamic acid decarboxylase, an enzyme that converts Glutamate to GABA. Therefore, the concurrent increase in the excitatory neurotransmitter, Glutamate, and decrease in inhibitory neurotransmitter, GABA, resultant from B6 deficiency, may manifest itself in the form of seizures.


==Pathophysiology==
==Causes==
[[File:Odd-chain_FA_oxydation.png|thumb|right|Methylmalonic acidemia is caused by a defect in the vitamin B<sub>12</sub>-dependent enzyme methylmalonyl CoA mutase.]]
*Supporters of a debated medical condition known as [[Pyroluria]] believe it may be one potential cause of vitamin B6 deficiency.  
*Another cause of vitamin B6 deficiency is the use of the tuberculostatic medication [[isoniazid]], and for this reason, it is recommended to supplement with vitamin B6 when using this drug. 
*Grumpiness and irritability are also often symptomatic of a deficiency according to "Body, Mind, and the B Vitamins" by Ruth Adams and Frank Murray.
*A [[meta-analysis]] of three databases ([[MEDLINE]], [[EMBASE]], and [[Cochrane Library]]), including only [[double-blind]], randomized controlled trials, found that vitamin B6 has a significant effect compared to [[placebo]]s in treating [[morning sickness]], similar to that of [[ginger]].<ref>[http://www.medicalnewstoday.com/medicalnews.php?newsid=22469 Pregnancy Morning Sickness - Ginger as Effective as Vitamin B6 (open)] [http://www.greenjournal.org/cgi/content/abstract/105/4/849 Effectiveness and Safety of Ginger in the Treatment of Pregnancy-Induced Nausea and Vomiting (subscription)], Borrelli ''et al.'',  ''Obstetrics & Gynecology'', 2005;105:849-856</ref>


In healthy individuals, the enzyme propionyl CoA carboxylase converts propionyl CoA to methylmalonyl CoA. This is one step in the process of converting certain [[amino acids]] and fats into sugar for energy. Individuals with PA cannot perform this conversion because the enzyme propionyl CoA carboxylase is nonfunctional. The essential amino acids [[isoleucine]], [[valine]], [[threonine]], and [[methionine]], as well as odd-chain [[fatty acids]], are simply converted to propionyl CoA, before the process stops, leading to a buildup of propionyl CoA. Instead of being converted to methylmalonyl CoA, propionyl CoA is then converted into [[propionic acid]], which builds up in the bloodstream. This in turn causes an accumulation of dangerous acids and toxins, which can cause damage to the organs.
===Diagnostic Testing for B6 Deficiency===
A positive diagnosis test for pyridoxine deficiency can be assertained by measuring [[erythrocyte]] levels of [[aspartate aminotransferase]] and transketolase in [[blood plasma|serum]].


In many cases, PA can damage the brain, heart, and liver, cause seizures, and delays to normal development like walking and talking. During times of illness the affected person may need to be hospitalized to prevent breakdown of proteins within the body. Each meal presents a challenge to those with PA. If not constantly monitored, the effects would be devastating. Dietary needs must be closely managed by a metabolic [[geneticist]] or metabolic [[dietician]].
== Differential Diagnosis ==
*Advanced Age
*Alcoholism
*Catabolic state
*[[Celiac Disease]]
*[[Chronic Renal Failure]]
*Drugs- [[Isoniazid]]
*Extrahepatic biliary obstruction
*Hemodialysis
*[[Hepatocellular Carcinoma]]
*[[Hepatitis]]
*Hospitalization
*Hyperoxaluria
*Kidney transplant
*Peritoneal dialysis
*Severe malnutrition <ref>Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:310</ref>


Mutations in both copies of the [[Propionyl-CoA carboxylase|PCCA]] or [[PCCB]] [[gene]]s cause propionic acidemia.<ref name="pamr">[http://mayoresearch.mayo.edu/mayo/research/barry_lab/ropionic-Aciademia.cfm http://mayoresearch.mayo.edu/mayo/research/barry_lab/ropionic-Aciademia.cfm]<br />Barry Lab - Vector and Virus Engineering. ''Gene therapy for Propionic Acidemia''</ref> These genes are responsible for the formation of the [[enzyme]] ''[[propionyl-CoA carboxylase]]'' ({{EC number|6.4.1.3}}), referred to as ''PCC''.
==References==
 
{{reflist|2}}
PCC is required for the normal breakdown of the essential amino acids valine, isoleucine, threonine, and methionine, as well as certain odd-chained fatty-acids. Mutations in the PCCA or PCCB genes disrupt the function of the enzyme, preventing these acids from being metabolized. As a result, [[propionyl-CoA]], propionic acid, [[ketones]], [[ammonia]], and other [[toxic]] compounds accumulate in the [[blood]], causing the signs and symptoms of propionic [[acidemia]].
 
==Symptoms==
Propionic acidemia is characterized almost immediately in newborns. Symptoms include poor feeding, [[vomiting]], [[dehydration]], [[acidosis]], low [[muscle]] tone ([[hypotonia]]), seizures, and [[lethargy]]. The effects of propionic acidemia quickly become life-threatening.
 
==Genetic prevalence==
 
[[Image:autorecessive.svg|thumb|right|Propionic acidemia has an autosomal recessive pattern of [[inheritance]].]]
 
Propionic acidemia is inherited in an [[autosomal]] [[recessive]] pattern and is found in about 1 in 35,000<ref name="pamr" /> live births in the [[United States]]. The condition appears to be more common in [[Saudi Arabia]],<ref name="pasa">{{cite journal |vauthors =Al-Odaib AN, Abu-Amaro KK, Ozand PT, Al-Hellani AM |title=A new era for preventive genetic programs in the Arabian Peninsula |journal=Saudi Medical Journal |volume=24 |issue=11 |pages=1168–1175 |year=2003 |pmid=14647548 }}</ref> with a frequency of about 1 in 3,000.<ref name="pamr" /> The condition also appears to be common in [[Amish]], [[Mennonite]] and other populations where inbreeding is common.<ref name="paam">{{cite journal |vauthors =Kidd JR, Wolf B, Hsia E, Kidd KK |title=Genetics of propionic acidemia in a Mennonite-Amish kindred |journal=Am J Hum Genet. |volume=32 |issue=2 |pages=236–245 |year=1980 |pmid=7386459 |pmc=1686010 }}</ref>
 
==Management==
Patients with propionic acidemia should be started as early as possible on a low protein diet. In addition to a protein mixture that is devoid of methionine, threonine, valine, and isoleucine, the patient should also receive L-carnitine treatment and should be given antibiotics 10 days per month in order to remove the intestinal propiogenic flora.  The patient should have diet protocols prepared for him with a “well day diet” with low protein content, a “half emergency diet” containing half of the protein requirements, and an “emergency diet” with no protein content. These patients are under the risk of severe hyperammonemia during infections that can lead to comatose states.<ref>Saudubray JM, Van Der Bergh G, Walter J : Inborn Metabolic Diseases Diagnosis and Treatment (2012)</ref>
 
Liver transplant is gaining a role in the management of these patients, with small series showing improved quality of life.


==See also==
* [[Methylmalonic acidemia]]
* [[Isovaleric acidemia]]
* [[Maple syrup urine disease]]
==References==
{{Reflist}}


==External links==
{{SIB}}
*[http://www.pafoundation.com  Propionic Acidemia Foundation]
{{Nutritional pathology}}
*[http://www.oaanews.org  Organic Acidemia Association]
*[http://www.paresearch.org  Propionic Acidemia Research Network (PARnet)]
*[http://www.gwenforacure.com Gwen for a Cure]
* {{NLM|propionicacidemia}}
*{{RareDiseases|467|Propionic acidemia}}
*{{cite web |url=http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=35 |title=Propionic acidemia |format= |work=Orphanet |accessdate=}}


{{Amino acid metabolic pathology}}
[[Category:Gastroenterology]]
{{Fatty-acid metabolism disorders}}


{{DEFAULTSORT:Propionic Acidemia}}
{{WikiDoc Help Menu}}
[[Category:Amino acid metabolism disorders]]
{{WikiDoc Sources}}
[[Category:Autosomal recessive disorders]]
[[Category:Rare diseases]]
[[Category:Fatty-acid metabolism disorders]]

Revision as of 14:02, 3 June 2016

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Overview

Vitamin B6 deficiency
ICD-10 E53.1
ICD-9 266.1
DiseasesDB 13923
eMedicine med/1977 
MeSH D026681

WikiDoc Resources for Sandbox/01

Articles

Most recent articles on Sandbox/01

Most cited articles on Sandbox/01

Review articles on Sandbox/01

Articles on Sandbox/01 in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Sandbox/01

Images of Sandbox/01

Photos of Sandbox/01

Podcasts & MP3s on Sandbox/01

Videos on Sandbox/01

Evidence Based Medicine

Cochrane Collaboration on Sandbox/01

Bandolier on Sandbox/01

TRIP on Sandbox/01

Clinical Trials

Ongoing Trials on Sandbox/01 at Clinical Trials.gov

Trial results on Sandbox/01

Clinical Trials on Sandbox/01 at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Sandbox/01

NICE Guidance on Sandbox/01

NHS PRODIGY Guidance

FDA on Sandbox/01

CDC on Sandbox/01

Books

Books on Sandbox/01

News

Sandbox/01 in the news

Be alerted to news on Sandbox/01

News trends on Sandbox/01

Commentary

Blogs on Sandbox/01

Definitions

Definitions of Sandbox/01

Patient Resources / Community

Patient resources on Sandbox/01

Discussion groups on Sandbox/01

Patient Handouts on Sandbox/01

Directions to Hospitals Treating Sandbox/01

Risk calculators and risk factors for Sandbox/01

Healthcare Provider Resources

Symptoms of Sandbox/01

Causes & Risk Factors for Sandbox/01

Diagnostic studies for Sandbox/01

Treatment of Sandbox/01

Continuing Medical Education (CME)

CME Programs on Sandbox/01

International

Sandbox/01 en Espanol

Sandbox/01 en Francais

Business

Sandbox/01 in the Marketplace

Patents on Sandbox/01

Experimental / Informatics

List of terms related to Sandbox/01

The classic clinical syndrome for Pyridoxine deficiency (or B6 deficiency) is a seborrheic dermatitis-like eruption, atrophic glossitis with ulceration, angular cheilitis, conjunctivitis, intertrigo, and neurologic symptoms of somnolence, confusion, and neuropathy.[1]

Vitamin B6 is a co-factor for glutamic acid decarboxylase, an enzyme that converts Glutamate to GABA. Therefore, the concurrent increase in the excitatory neurotransmitter, Glutamate, and decrease in inhibitory neurotransmitter, GABA, resultant from B6 deficiency, may manifest itself in the form of seizures.

Causes

  • Supporters of a debated medical condition known as Pyroluria believe it may be one potential cause of vitamin B6 deficiency.
  • Another cause of vitamin B6 deficiency is the use of the tuberculostatic medication isoniazid, and for this reason, it is recommended to supplement with vitamin B6 when using this drug.
  • Grumpiness and irritability are also often symptomatic of a deficiency according to "Body, Mind, and the B Vitamins" by Ruth Adams and Frank Murray.
  • A meta-analysis of three databases (MEDLINE, EMBASE, and Cochrane Library), including only double-blind, randomized controlled trials, found that vitamin B6 has a significant effect compared to placebos in treating morning sickness, similar to that of ginger.[2]

Diagnostic Testing for B6 Deficiency

A positive diagnosis test for pyridoxine deficiency can be assertained by measuring erythrocyte levels of aspartate aminotransferase and transketolase in serum.

Differential Diagnosis

References

  1. ↑ Andrews' Diseases of the Skin, 10th Edition, Elsevier.
  2. ↑ Pregnancy Morning Sickness - Ginger as Effective as Vitamin B6 (open) Effectiveness and Safety of Ginger in the Treatment of Pregnancy-Induced Nausea and Vomiting (subscription), Borrelli et al., Obstetrics & Gynecology, 2005;105:849-856
  3. ↑ Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:310


Template:SIB Template:Nutritional pathology


Template:WikiDoc Sources

Retrieved from "https://www.wikidoc.org/index.php?title=Sandbox/01&oldid=1234287"