Evidence map›Paper›PMID 37377459›Full record

ArticleSAGE open medical case reports2023

Arginase deficiency with parotid gland swelling and hyperamylasemia: A case report.

Noboru Kuyama, Shigeru Nagaki, Akie Miyamoto, Kaoru Etou, Hiroshi Maruyama, Makiko Osawa

Open access · goldAbstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 85% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Noboru KuyamaDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Shigeru NagakiDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0627-1368
Akie MiyamotoDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Kaoru EtouDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Hiroshi MaruyamaDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Makiko OsawaDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Tokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arginase deficiency is a progressive neurological disorder characterized by episodic hyperammonemia crises. Our patient had been diagnosed with cerebral palsy (spastic paraplegia) in childhood and received rehabilitation. She had suffered parotid swelling since the age of 5 years, prior to liver dysfunction becoming apparent, and then developed hyperamylasemia at 8 years of age. At age 25 years, she presented with hyperammonemia and elevations of aspartate aminotransferase and alanine aminotransferase. At age 27 years, she was diagnosed with arginase deficiency due to hyperargininemia and absent arginase activity in erythrocytes. Liver cirrhosis was also present. She was hospitalized several times for management of episodic hyperammonemia due to recurrent viral infections, an unbalanced diet, and poor compliance with medications.

Indexed as

Arginase deficiencyhyperammonemiahyperamylasemialiver cirrhosisparotid gland swelling

Identifiers

PMID37377459
PMCPMC10291395
OpenAlexW4381889802

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.