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Diagnostic and treatment implications of psychosis secondary to treatable metabolic disorders in adults: a systematic review

Orphanet Journal of Rare Diseases

Apr 30, 2014

Olivier BonnotMark Walterfang

Abstract

It is important for psychiatrists to be aware of certain inborn errors of metabolism (IEMs) as these rare disorders can present as psychosis, and because definitive treatments may be available for treating the underlying metabolic cause. A systematic review was conducted to examine IEMs...read more

Mentioned in this Paper

Metabolic Process, Cellular
Inborn Errors of Metabolism
Niemann-Pick Disease, Type C
Acute Intermittent Porphyria
Schizophrenia
Deficiency of Reductase
Homocysteinemia
Homocysteine Metabolic Process
5,10-Methylenetetrahydrofolate Reductase Deficiency
Hyperhomocysteinemia
7
1
121
1
Paper Details
References
  • References102
  • Citations14
12345...
  • References102
  • Citations14
12

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Diagnostic and treatment implications of psychosis secondary to treatable metabolic disorders in adults: a systematic review

Orphanet Journal of Rare Diseases

Apr 30, 2014

Olivier BonnotMark Walterfang

PMID: 24775716

DOI: 10.1186/1750-1172-9-65

Abstract

It is important for psychiatrists to be aware of certain inborn errors of metabolism (IEMs) as these rare disorders can present as psychosis, and because definitive treatments may be available for treating the underlying metabolic cause. A systematic review was conducted to examine IEMs...read more

Mentioned in this Paper

Metabolic Process, Cellular
Inborn Errors of Metabolism
Niemann-Pick Disease, Type C
Acute Intermittent Porphyria
Schizophrenia
Deficiency of Reductase
Homocysteinemia
Homocysteine Metabolic Process
5,10-Methylenetetrahydrofolate Reductase Deficiency
Hyperhomocysteinemia
7
1
121
1

Similar Papers Found In These Feeds

Rasmussen's Syndrome

Rasmussen syndrome typically occurs in children and is characterized by the development of intractable focal seizures, progressive hemiparesis, and intellectual deterioration. Discover the latest research on Rasmussen syndrome here.

Wilson Disease

Wilson’s disease is an autosomal recessive disorder caused by mutation in the ATP7B gene and is characterized by copper build-up in the body. Discover the latest research on Wilson’s disease here.

Related Papers

Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie

Behavior and psychiatric symptoms: intoxication diseases in inborn errors of metabolism

Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrieJuly 27, 2010
F LabartheFrançois Maillot
Paper Details
References
  • References102
  • Citations14
12345...
  • References102
  • Citations14
12
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