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

Study acronym: AlBaathU
StatusUnknown
PhaseNot specified
Started

Record status This record was last updated September 27, 2024 (before its estimated September 12, 2025 completion). Its status may not reflect the trial's current state.

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Record History

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  1. Changed Registry marked status Unknown (sponsor has not verified the record since Sep 2024); last known: Not Yet Recruiting
  2. Study description shortened, about 10 words
    • Publications: details revised at 6 of 6 entries
    v2
  3. Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06615011
Lead Sponsor Al Baath University
Conditions
(from sponsor)		 Bardet Biedl Syndrome (BBS)
Related terms Bardet-Biedl Syndrome, Obesity, Abdominal, Polydactyly, Postaxial
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov