Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity

    Ahmed H. Nouh, Fatma Elgendy, Fatma Gobran, Maryna Zhuravlova
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    TLDR Genetic testing is crucial for diagnosing rare hair loss disorders.
    This study reports the first case series of Marie Unna hereditary hypotrichosis (MUHH) in Egypt, involving two unrelated families. It identifies two heterozygous pathogenic variants in the HRURF gene, contributing to the understanding of genotype–phenotype correlations in this rare disorder. The research highlights the clinical variability of MUHH, with unique hair loss patterns and dermoscopic findings. It underscores the importance of genetic testing for diagnosis and calls for further functional studies to explore the HRURF gene's role in hair development and cycling, which may lead to effective treatments.
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