Evidence map›Paper›PMID 38076312›Full record

ArticleJournal of surgical case reports2023

Urethral reconstruction using amniotic membrane allograft in hereditary androgen insensitivity syndrome: a case series.

Marah Mansour, Maria Raya, Abd Alrahman Jrdy, Abdoul Majid Sires, Jad Alhaq Wardeh, Almoataz Ballah Alsbekhan, Sabah Faour, Mahmoud Kanas, Mhd Firas Safadi, Khaled Alrebdawi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of surgical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

10 authors at 7 institutions in 3 countries.

Marah MansourFaculty of Medicine, Tartous University, Tartous 95747, Syrian Arab Republic.
Maria RayaFaculty of Medicine, University of Kalamoon, Damascus, Syrian Arab Republic.ORCID https://orcid.org/0000-0003-1402-3935
Abd Alrahman JrdyFaculty of Medicine, Tishreen University, Latakia, Syrian Arab Republic.ORCID https://orcid.org/0000-0003-4287-7882
Abdoul Majid SiresFaculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.ORCID https://orcid.org/0000-0003-4229-1830
Jad Alhaq WardehFaculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.
Almoataz Ballah AlsbekhanFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Sabah FaourFaculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.
Mahmoud KanasFaculty of Medicine, Yuzuncu Yil University, Van, Turkey.
Mhd Firas SafadiDepartment of General and Visceral Surgery, Erzgebirgsklinikum Annaberg, Annaberg-Buchholz 09456, Germany.
Khaled AlrebdawiDepartment of Urological Surgery, Surgical Kidney Hospital, Damascus, Syrian Arab Republic.
University of Aleppo · SYDamascus Hospital · SYDamascus University · SYKlinikum Arnsberg · DELatakia University · SYUniversity of Kalamoon · SYVan Yüzüncü Yıl Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Partial androgen insensitivity syndrome is a rare X-linked disorder. While most cases are sporadic, familial cases are less frequent. The management of this syndrome follows a multidisciplinary approach involving hormone substitution, psychological counseling, and surgical procedures. We present a case series of three young siblings with familial partial androgen insensitivity syndrome who presented with a female phenotype. All of them were managed with hormonal treatment for 6 months followed by surgical reconstruction. The operative procedure involved phalloplasty and urethroplasty using amniotic membrane transplant, which is considered a novel technique in this group of patients. No intraoperative or postoperative complications were observed and good results were achieved within 2 years of follow-up.

Indexed as

amniotic membrane allograftandrogen insensitivity syndromeandrogen receptor insensitivity syndromegender transitionsexual development

Identifiers

PMID38076312
PMCPMC10702271
OpenAlexW4389454553

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.