Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder

Purine nucleoside phosphorylase (PNP) deficiency is one of the very rare types of immune deficiency disorders inherited in an autosomal recessive (AR) manner. PNP deficiency is a progressive immune disorder that can range from severe combined immunodeficiency (SCID) to combined immunodeficiency and is associated with recurrent infections, neurological manifestations, and sometimes autoimmune disorders. In our case, we describe the case of a female patient, two years and six months old, with recurrent infections, severe neutropenia, failure to thrive, and a history of a deceased sister with the same condition. She was diagnosed with PNP through genetic testing, which confirmed the homozygous variant c.46T>C p.(Trp16Arg) in PNP, in addition to clinical manifestations and the positive history of her sister.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2024-12-22
DOI
https://doi.org/10.7759/cureus.76220
Citations
1
Primary Topic
Biochemical and Molecular Research
Type
article
Field-Weighted Citation Impact
0.23
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder

Badriah G Alasmari, Muhammad Saeed, Abdullah Alshehri, Shady Wafa et al.
1 citations
Cureus
Biochemical and Molecular Research
0.23
article

Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder

Badriah G Alasmari, Muhammad Saeed, Abdullah Alshehri, Shady Wafa, Fady Ibrahim
article en
1 citations

Abstract

Purine nucleoside phosphorylase (PNP) deficiency is one of the very rare types of immune deficiency disorders inherited in an autosomal recessive (AR) manner. PNP deficiency is a progressive immune disorder that can range from severe combined immunodeficiency (SCID) to combined immunodeficiency and is associated with recurrent infections, neurological manifestations, and sometimes autoimmune disorders. In our case, we describe the case of a female patient, two years and six months old, with recurrent infections, severe neutropenia, failure to thrive, and a history of a deceased sister with the same condition. She was diagnosed with PNP through genetic testing, which confirmed the homozygous variant c.46T>C p.(Trp16Arg) in PNP, in addition to clinical manifestations and the positive history of her sister.

CureusVol. 16(12)
Armed Forces Hospital (SA)
Openalex Percentile: Top 40%
Biochemical and Molecular Research
0.23
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder — Badriah G Alasmari, Muhammad Saeed, et al. · Cureus (2024) | TGRS Research Map | TGRS