Purine nucleoside phosphorylase deficiency

Purine nucleoside phosphorylase deficiency
Synonyms	PNP-deficiency
Pronounce	N/A
Field	N/A
Symptoms	N/A
Complications
Onset
Duration
Types
Causes
Risks
Diagnosis
Differential diagnosis
Prevention
Treatment	Allegeneic hemotopoietic stem cell transplantation (HSCT)
Medication
Prognosis
Frequency
Deaths

Purine nucleoside phosphorylase deficiency, is a rare autosomal recessive<ref name=pnpar>,

 Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient, 
 Human Genetics, 
 
 Vol. 103(Issue: 1),
 pp. 81–85,
 DOI: 10.1007/s004390050787,
 PMID: 9737781,</ref> metabolic disorder which results in immunodeficiency.

Signs and symptoms

In addition to the symptoms associated with immunodeficiency, such as depletion of T-cells, decline of lymphocyte activity, and an abrupt proliferation of both benign and opportunistic infections — PNP-deficiency is often characterized by the development of autoimmune disorders. lupus erythematosus, autoimmune hemolytic anemia, and idiopathic thrombocytopenic purpura have been reported with PNP-deficiency.<ref name="pnpone">Markert ML,

 Purine nucleoside phosphorylase deficiency, 
 Immunodefic Rev., 
 1991,
 Vol. 3(Issue: 1),
 pp. 45–81,
 
 PMID: 1931007,</ref>

Neurological symptoms, such as developmental decline, hypotonia, and mental retardation have also been reported.

Cause

The disorder is caused by a mutation of the purine nucleoside phosphorylase (PNP) gene, located at chromosome 14q13.1.<ref>Online Mendelian Inheritance in Man (OMIM) 164050 </ref><ref name="pmid9122228"/> This mutation was first identified by Eloise Giblett, a professor at the University of Washington, in 1975.<ref>Motulsky A, Gartler S. "Biographical Memoirs: Eloise R. Giblett". National Academy of Sciences.</ref> PNP is a key enzyme in the purine catabolic<ref>,

 Biochemistry, 
 7th edition, 
  
  
  
  
 ISBN 9781429229364,</ref> pathway, and is required for purine degradation. Specifically, it catalyzes the conversion of inosine to hypoxanthine and guanosine to guanine (both guanine and hypoxanthine will be made into xanthine which will then become uric acid). A deficiency of it leads to buildup of elevated deoxy-GTP (dGTP) levels resulting in T-cell toxicity and deficiency.<ref name="pmid9122228">, 
 Point mutations at the purine nucleoside phosphorylase locus impair thymocyte differentiation in the mouse, 
 Proc. Natl. Acad. Sci. U.S.A., 
 
 Vol. 94(Issue: 6),
 pp. 2522–2527,
 DOI: 10.1073/pnas.94.6.2522,
 PMID: 9122228,
 PMC: 20121,</ref><ref name="pmid16964310">, 
 TAT-mediated intracellular delivery of purine nucleoside phosphorylase corrects its deficiency in mice, 
 J. Clin. Invest., 
 
 Vol. 116(Issue: 10),
 pp. 2717–2726,
 DOI: 10.1172/JCI25052,
 PMID: 16964310,
 PMC: 1560347,</ref> In contrast to adenosine deaminase deficiency (another deficiency of purine metabolism), there is minimal disruption to B cells.<ref name="urleMedicine - Purine Nucleoside Phosphorylase Deficiency : Article by Alan P Knutsen">

eMedicine - Purine Nucleoside Phosphorylase Deficiency : Article by Alan P Knutsen(link). {{{website}}}.

</ref>

PNP deficiency is inherited in an autosomal recessive manner.<ref name=pnpar/> This means the defective gene responsible for the disorder is located on an autosome (chromosome 14 is an autosome), and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

Diagnosis

Diagnostic methods

Diagnosis is based on the clinical examination and on laboratory findings showing leukopenia, severe lymphopenia with low CD3, CD4, and CD8 counts and variable B cell function and immunoglobulin levels. Neutropenia has also been reported. Hallmark diagnostic markers of PNP deficiency include hypouricemia, complete or near complete absence of PNP activity in red blood cell lysate and increased urine or blood levels of inosine, guanosine and their deoxy forms. Diagnosis is confirmed by genetic screening of PNP.

Differential diagnosis

Differential diagnosis includes aplastic anemias, SCID, severe combined immunodeficiency due to adenosine deaminase deficiency, ataxia-telangiectasia, and viral meningoencephalitis.

Antenatal diagnosis

Measurement of T cell receptor excision circles during newborn screening for SCID can detect some patients suffering from PNP deficiency, although removal of metabolites by maternal PNP may delay the deleterious effects on PNP-deficient lymphocytes. Few newborn screening programs also measure purine metabolites in dried

Treatment

Supportive treatment, including intravenous immunoglobulin therapy, prophylaxis for Pneumocystis carinii, and physical, occupational, and speech therapy, reduces the risk of infection and may encourage optimal neurologic development for patients.

Epidemiology

PNP-deficiency is extremely rare. Only 33 patients with the disorder in the United States have been documented.<ref name="pnpone"/> In the United Kingdom only two children have been diagnosed with this disorder in 1994 and 2008.<ref>http://www.channel4.com/news/articles/society/health/boy+first+in+uk+with+rare+condition/3022087</ref>

See also

• Nezelof syndrome

External links

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  Diagram illustrating autosomal recessive inheritance pattern.