Evidence map›Paper›PMID 42750964›Full record

ArticleClinical case reports2026

Recognition of Patau Syndrome (Trisomy 13) Based on Clinical Features in a Resource-Limited Setting: A Case Report.

Sayed Hussain Amiri, Nasir Ahmad Anwari, Dawood Hossaini, Abdulhaq Qiam, Murtaza Haidary

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In one paragraph

Article in Clinical case reports, 2026. 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
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.

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

5 authors.

Sayed Hussain AmiriDepartment of Paraclinic, Faculty of Curative Medicine Shifa University Kabul Afghanistan.ORCID https://orcid.org/0009-0001-3595-5531
Nasir Ahmad AnwariDepartment of Pediatric Medicine Atatürk Children's Hospital Kabul Afghanistan.
Dawood HossainiDepartment of Paraclinical Sciences and Laboratory Management, Faculty of Medical Laboratory Technology Khatam Al-Nabieen University Kabul Afghanistan.
Abdulhaq QiamDepartment of Pediatric Medicine Atatürk Children's Hospital Kabul Afghanistan.
Murtaza HaidaryMedical Research and Technology Center Khatam Al-Nabieen University Kabul Afghanistan.ORCID https://orcid.org/0000-0002-7273-9088

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patau syndrome (trisomy 13) is a life-limiting chromosomal disorder with multiple congenital anomalies. We report a term male neonate with bilateral cleft lip and palate, aplasia cutis congenita, postaxial polydactyly, hypotonia, congenital heart disease, and presumed neonatal sepsis. Clinical diagnosis was made without cytogenetic confirmation; the infant died on day five.

Indexed as

aplasia cutis congenitacleft lip and palatecongenital anomaliescongenital heart diseaseneonatePatau syndromepostaxial polydactylytrisomy 13

Identifiers

PMID42750964
PMCPMC13578909

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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 OpenQuestion graph.