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1.
Arch Iran Med ; 26(12): 712-716, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-38431953

ABSTRACT

Two Iranian patients with purine nucleoside phosphorylase (PNP) deficiency are described in terms of their clinical and molecular evaluations. PNP deficiency is a rare form of combined immunodeficiency with a profound cellular defect. Patients with PNP deficiency suffer from variable recurrent infections, hypouricemia, and neurological manifestations. Furthermore, patient 1 developed mild cortical atrophy, and patient 2 presented developmental delay, general muscular hypotonia, and food allergy. The two unrelated patients with developed autoimmune hemolytic anemia and T cells lymphopenia and eosinophilia were referred to Immunology, Asthma and Allergy Research Institute (IAARI) in 2019. After taking blood and DNA extraction, genetic analysis of patient 1 was performed by PCR and direct sequencing and whole exome sequencing was applied for patient 2 and the result was confirmed by direct sequencing in the patient and his parents. The genetic result showed two novel variants in exon 3 (c.246_285+9del) and exon 5 (c.569G>T) PNP (NM_000270.4) in the patients, respectively. These variants are considered likely pathogenic based on the American College of Medical Genetics and Genomics (ACMG) guideline. PNP deficiency has a poor prognosis; therefore, early diagnosis would be vital to receive hematopoietic stem cell transplantation (HSCT) as a prominent and successful treatment.


Subject(s)
Anemia, Hemolytic, Autoimmune , Primary Immunodeficiency Diseases , Purine-Nucleoside Phosphorylase , Humans , Anemia, Hemolytic, Autoimmune/genetics , Eosinophilia/genetics , Iran , Mutation , Purine-Nucleoside Phosphorylase/genetics , Purine-Nucleoside Phosphorylase/deficiency , Purine-Pyrimidine Metabolism, Inborn Errors/genetics
2.
Rev. chil. nutr ; 26(2): 195-200, ago. 1999. tab
Article in Spanish | LILACS | ID: lil-286837

ABSTRACT

Se analiza las consecuencias provocadas por desequilibrios nutricionales sobre el contenido de DNA y la actividad de las enzimas ADA y PNP en timo de ratas en crecimientos. Ratas Wistar al destete fueron alimentadas con: 1- dieta libre de proteínas hasta asemejar cuadros de malnutrición proteica leve, moderada y severa; 2- dieta conteniendo harina de maíz en baja concentración (6,5 por ciento). La subnutrición durante la lactancia se obtuvo duplicando la camada (12-14 crías por madre). Como controles se utilizaron ratas bien nutridas de igual edad, que desde el destete recibieron dieta stock. Al finalizar la experiencia, se les extrajo el timo (Pt)(mg). Se determinó DNA (mg/órgano), el número de núcleos, el tamaño celular- Pt(mg)/No. de Núcleos- y la actividad de las enzimas ADA y PNP (umol de ácido úrico x 10 - 1/P)(P=Pt(mg) /P corporal 0.75). Los resultados muestran que tanto la subnutrición durante la lactancia, como la malnutrición proteica al destete y la administración de dieta de baja calidad, afectan la proliferación celular en el timo, Sólo la carencia de proteína o su baja calidad, aumenta la actividad de ADA y PNP


Subject(s)
Animals , Rats , Protein Deficiency/enzymology , Protein-Energy Malnutrition/enzymology , Adenosine Deaminase/deficiency , Adenosine Deaminase/pharmacology , Diet, Protein-Restricted/adverse effects , Purine-Nucleoside Phosphorylase/deficiency , Purine-Nucleoside Phosphorylase/pharmacology , Rats, Wistar/growth & development , Sequence Analysis, DNA , Thymus Gland/enzymology
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