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NCT06615011: AlBaathU

Bardet Beidle Syndrome in a Syrian Adolescent : a Rare Case Report

Not yet recruiting Last updated 27 September 2024
What this trial tests

trial in Bardet Biedl Syndrome (BBS) in 100 participants. Not yet recruiting.

Timeline
12 October 2024
Primary endpoint
12 September 2025
12 October 2025

Quick facts

Lead sponsorAl Baath University
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment100
Start date12 October 2024
Primary completion12 September 2025
Estimated completion12 October 2025

Conditions studied

Sponsor

Al Baath University

Who can join

Eligibility, any sex, with Bardet Biedl Syndrome (BBS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Bardet-Biedl Syndrome (BBS) is an uncommon genetic disorder that affects multiple organs. and presents with a variety of characteristics. It is caused by a dysfunction in the cilia. We present a case of bradet-biedl syndrome presenting with intellectual disabilities, post-axial polydactyly, gingival hyperplasia, and a significant family history of scleroderma. The diagnosis was determined based on clinical physical examination findings. The patient is undergoing treatment with Thyroxine. Although medical staff are incapable of treatment, systems support adjust the overall well-being and quality of life for individuals with Bardet-Biedl syndrome and their families.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Bardet-Biedl syndrome in a Syrian adolescent: a rare case report.
    Alabed A, Alhallak S, Dakkak T, Alhaj Ali AJ, et al · · 2025 · PMID 40486581 · DOI 10.1097/ms9.0000000000003077

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