Evidence map›Paper›PMID 37974760›Full record

ArticleIndian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India2023

Hearing Loss with Vision Impairment: Usher Syndrome. A Case of the East Democratic Republic of Congo.

Amani Mudekereza Edouard, Nshokano Simba Gloria, Ahmed Youssef Sobhi, Amani Muzindusi Christian, Kabego Kulimushi Fidele, Murhula Mulumeoderhwa Fabrice, Balaluka Mulinganya Christian, Ngoma Basedeke Deogratias, Balungwe Birindwa Patrick

Open access · greenAbstract read
In one paragraph

Article in Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India, 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
0.2field-weighted citation impact, top 49% 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, 1 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

9 authors at 2 institutions in 2 countries.

Amani Mudekereza EdouardDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Université Catholique de Bukavu(UCB), Bukavu, Democratic Republic of the Congo.ORCID 0000-0001-6399-7352
Nshokano Simba GloriaOtothinolaryngology ward and Ophtamology Ward, Hopital Provincial General de Référence de Bukavu (HPGRB), Bukavu, Democratic Republic of the Congo.
Ahmed Youssef SobhiDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Amani Muzindusi ChristianDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Université Catholique de Bukavu(UCB), Bukavu, Democratic Republic of the Congo.
Kabego Kulimushi FideleOtothinolaryngology ward and Ophtamology Ward, Hopital Provincial General de Référence de Bukavu (HPGRB), Bukavu, Democratic Republic of the Congo.
Murhula Mulumeoderhwa FabriceDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Université Catholique de Bukavu(UCB), Bukavu, Democratic Republic of the Congo.
Balaluka Mulinganya ChristianDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Université Catholique de Bukavu(UCB), Bukavu, Democratic Republic of the Congo.
Ngoma Basedeke DeogratiasOtothinolaryngology ward and Ophtamology Ward, Hopital Provincial General de Référence de Bukavu (HPGRB), Bukavu, Democratic Republic of the Congo.
Balungwe Birindwa PatrickDepartment of Otorhinolaryngology Head and Neck Surgery, Faculty of Medicine, Université Catholique de Bukavu(UCB), Bukavu, Democratic Republic of the Congo.
Université Catholique de Bukavu · CDAlexandria University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Usher syndrome (USH) is a clinically heterogeneous condition characterized by sensorineural hearing loss, progressive retinal degeneration, and vestibular dysfunction. There are two phenotypically recognizable types of Usher syndrome described in the literature. Usher type 1 individual have no vestibular function and profound sensorineural hearing loss. Usher type 2 individuals have a normal vestibular function and mild-to-severe hearing loss with visual impairment that is presented later in life. We are reporting a case of 35 years old gentleman with hearing loss and visual impairment presented to the ENT clinic at the tertiary care center. Clinical evaluations as well as comprehensive testing of hearing, vestibular function, and visual function have confirmed USH. It's a rare but serious cause of hearing loss that requires comprehensive multidisciplinary evaluation in conjunction with an ophthalmology team. Further genetic, audiological, and vestibular assessments are required to help diagnose and management of specific subtypes of this syndrome. Supplementary Information: The online version contains supplementary material available at 10.1007/s12070-023-03970-4.

Indexed as

Autosomal recessiveCongo democraticRetinitis pigmentosaUsher’s syndrome

Identifiers

PMID37974760
PMCPMC10646019
OpenAlexW4384562132

What OpenQuestion holds

Textmetadata
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.