DSG4 Gene Variants as a Cause of Hypotrichosis in a Child with Severe Atopic Dermatitis: Clinical Case

    Nikolay N. Murashkin, Roman V. Epishev, Olesya D. Dubenko … М. А. Леонова
    Studysummary This study reported that genetic testing is crucial for accurately diagnosing hypotrichosis, especially in cases with subtle symptoms or coexisting severe atopic dermatitis, as demonstrated in a young girl with a DSG4 gene mutation.
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    Research cited in this study 8

    1. Treatment of Hereditary Hypotrichosis Simplex of the Scalp with Oral Minoxidil and Growth Factors Dermatologic Therapy · 2022
    2. Isolated Autosomal Recessive Woolly Hair/Hypotrichosis: Genetics, Pathogenesis, and Therapies JEADV. Journal of the European Academy of Dermatology and Venereology/Journal of the European Academy of Dermatology and Venereology · 2021
    3. Association of Alopecia Areata with Atopic Dermatitis and Chronic Spontaneous Urticaria Allergy and asthma proceedings · 2018
    4. Therapeutic Potential of Bimatoprost for the Treatment of Eyebrow Hypotrichosis Drug Design Development and Therapy · 2018
    5. Bimatoprost for the Treatment of Eyelash, Eyebrow, and Scalp Alopecia Expert Opinion on Investigational Drugs · 2017
    6. Novel D323G Mutation of DSG4 Gene in a Girl with Localized Autosomal Recessive Hypotrichosis Clinically Overlapped with Monilethrix International Journal of Dermatology · 2015
    7. Congenital Atrichia and Hypotrichosis World Journal of Pediatrics · 2011
    8. Marie-Unna Hereditary Hypotrichosis: Case Report and Review of the Literature Pediatric dermatology · 2011

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