A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 and Non-Ossifying Fibroma in Femur: A Case Report

    August 2022 in “ Journal of Comprehensive Pediatrics ”
    Aye Miremarati, Manijeh Tabrizi, Setila Dalili, Seyyedeh Azade Hoseini Nouri
    Studysummary This case report describes a 15-year-old girl with trichorhinophalangeal syndrome type 1 and a rare non-ossifying fibroma in her femur, suggesting a potential link between the genetic condition and bone lesions.
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    Research cited in this study 4

    1. Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report Skin appendage disorders · 2020
    2. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019
    3. An Early Diagnosis of Trichorhinophalangeal Syndrome Type 1: A Case Report and Review of Literature ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 2018
    4. Treatment of Hair Loss in the Trichorhinophalangeal Syndrome Annals of dermatology/Annals of Dermatology · 2018