Urea cycle disorder--argininosuccinic lyase deficiency.
Identifieur interne : 000269 ( Main/Exploration ); précédent : 000268; suivant : 000270Urea cycle disorder--argininosuccinic lyase deficiency.
Auteurs : Neeta Mehta [États-Unis] ; Pia Chatterjee Kirk ; Ray Holder ; Harry V. PrecheurSource :
- Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry [ 1754-4505 ]
Descripteurs français
- KwdFr :
- Acidurie arginosuccinique (anatomopathologie), Acidurie arginosuccinique (complications), Acidurie arginosuccinique (enzymologie), Cytochrome P-450 CYP3A (métabolisme), Humains (MeSH), Hyperammoniémie (complications), Interactions médicamenteuses (MeSH), Maladies de la bouche (thérapie), Maladies de la bouche (étiologie), Préparations pharmaceutiques en odontologie (effets indésirables), Soins dentaires pour malades chroniques (MeSH).
- MESH :
- anatomopathologie : Acidurie arginosuccinique.
- effets indésirables : Acidurie arginosuccinique, Hyperammoniémie, Préparations pharmaceutiques en odontologie.
- enzymologie : Acidurie arginosuccinique.
- métabolisme : Cytochrome P-450 CYP3A.
- thérapie : Maladies de la bouche.
- étiologie : Maladies de la bouche.
- Humains, Interactions médicamenteuses, Soins dentaires pour malades chroniques.
English descriptors
- KwdEn :
- Argininosuccinic Aciduria (complications), Argininosuccinic Aciduria (enzymology), Argininosuccinic Aciduria (pathology), Cytochrome P-450 CYP3A (metabolism), Dental Care for Chronically Ill (MeSH), Drug Interactions (MeSH), Humans (MeSH), Hyperammonemia (complications), Mouth Diseases (etiology), Mouth Diseases (therapy), Pharmaceutical Preparations, Dental (adverse effects).
- MESH :
- chemical , adverse effects : Pharmaceutical Preparations, Dental.
- chemical , metabolism : Cytochrome P-450 CYP3A.
- complications : Argininosuccinic Aciduria, Hyperammonemia.
- enzymology : Argininosuccinic Aciduria.
- etiology : Mouth Diseases.
- pathology : Argininosuccinic Aciduria.
- therapy : Mouth Diseases.
- Dental Care for Chronically Ill, Drug Interactions, Humans.
Abstract
An increased level of ammonia in the bloodstream, or hyperammonemia, is a symptom associated with metabolic disorders referred to as inborn errors of metabolism. Urea cycle disorder is a congenital abnormality or absence of one of the six enzymes involved in the elimination of ammonia. Administration of certain medications, high protein diet, excessive exercise, surgical procedures, or trauma can precipitate symptoms of mental confusion, seizure-like activity, and ataxia. This paper reviews the literature with insight into current treatment and management options of the disorder and modification of treatment for the dental patient.
DOI: 10.1111/j.1754-4505.2012.00263.x
PubMed: 22784324
Affiliations:
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Urea cycle disorder is a congenital abnormality or absence of one of the six enzymes involved in the elimination of ammonia. Administration of certain medications, high protein diet, excessive exercise, surgical procedures, or trauma can precipitate symptoms of mental confusion, seizure-like activity, and ataxia. This paper reviews the literature with insight into current treatment and management options of the disorder and modification of treatment for the dental patient.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22784324</PMID><DateCompleted><Year>2013</Year><Month>01</Month><Day>02</Day></DateCompleted><DateRevised><Year>2012</Year><Month>07</Month><Day>12</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1754-4505</ISSN><JournalIssue CitedMedium="Internet"><Volume>32</Volume><Issue>4</Issue><PubDate><MedlineDate>2012 Jul-Aug</MedlineDate></PubDate></JournalIssue><Title>Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry</Title><ISOAbbreviation>Spec Care Dentist</ISOAbbreviation></Journal><ArticleTitle>Urea cycle disorder--argininosuccinic lyase deficiency.</ArticleTitle><Pagination><MedlinePgn>155-9</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1754-4505.2012.00263.x</ELocationID><Abstract><AbstractText>An increased level of ammonia in the bloodstream, or hyperammonemia, is a symptom associated with metabolic disorders referred to as inborn errors of metabolism. Urea cycle disorder is a congenital abnormality or absence of one of the six enzymes involved in the elimination of ammonia. Administration of certain medications, high protein diet, excessive exercise, surgical procedures, or trauma can precipitate symptoms of mental confusion, seizure-like activity, and ataxia. This paper reviews the literature with insight into current treatment and management options of the disorder and modification of treatment for the dental patient.</AbstractText><CopyrightInformation>© 2012 Special Care Dentistry Association and Wiley Periodicals, Inc.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mehta</LastName><ForeName>Neeta</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Department of Advanced Dentistry, School of Dentistry, University of Mississippi, Jackson, Mississippi, USA. nmehta@umc.edu</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kirk</LastName><ForeName>Pia Chatterjee</ForeName><Initials>PC</Initials></Author><Author ValidYN="Y"><LastName>Holder</LastName><ForeName>Ray</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Precheur</LastName><ForeName>Harry V</ForeName><Initials>HV</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Spec Care Dentist</MedlineTA><NlmUniqueID>8103755</NlmUniqueID><ISSNLinking>0275-1879</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D053210">Pharmaceutical Preparations, Dental</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.14.14.1</RegistryNumber><NameOfSubstance UI="D051544">Cytochrome P-450 CYP3A</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D056807" MajorTopicYN="Y">Argininosuccinic Aciduria</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051544" MajorTopicYN="N">Cytochrome P-450 CYP3A</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017742" MajorTopicYN="Y">Dental Care for Chronically Ill</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004347" MajorTopicYN="N">Drug Interactions</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D022124" MajorTopicYN="N">Hyperammonemia</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009059" MajorTopicYN="N">Mouth Diseases</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053210" MajorTopicYN="N">Pharmaceutical Preparations, Dental</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="Y">adverse effects</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>7</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>7</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2013</Year><Month>1</Month><Day>3</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">22784324</ArticleId><ArticleId IdType="doi">10.1111/j.1754-4505.2012.00263.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>État du Mississippi</li></region></list><tree><noCountry><name sortKey="Holder, Ray" sort="Holder, Ray" uniqKey="Holder R" first="Ray" last="Holder">Ray Holder</name><name sortKey="Kirk, Pia Chatterjee" sort="Kirk, Pia Chatterjee" uniqKey="Kirk P" first="Pia Chatterjee" last="Kirk">Pia Chatterjee Kirk</name><name sortKey="Precheur, Harry V" sort="Precheur, Harry V" uniqKey="Precheur H" first="Harry V" last="Precheur">Harry V. Precheur</name></noCountry><country name="États-Unis"><region name="État du Mississippi"><name sortKey="Mehta, Neeta" sort="Mehta, Neeta" uniqKey="Mehta N" first="Neeta" last="Mehta">Neeta Mehta</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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