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Arch Dermatol Res ; 316(7): 438, 2024 Jun 28.
Article in English | MEDLINE | ID: mdl-38940945

ABSTRACT

Dyskeratosis congenita (DC) is a telomeropathy presenting diagnostic and therapeutic challenges across multiple specialties; yet, subtle dermatological signs enable early detection, altering patient prognosis. A specific DC genetic sequencing was performed according to the clinical criteria of our patient in study. Subsequently, cross-checked information in the main genetic databases was carried out. Additionally, an extensive review of the literature was made to organize the main dermatological aspects in DC. We report a novel variant of DC. Additionally, we share 10 useful and practical messages for dermatologists and any specialist caring for this group of patients.


Subject(s)
Dyskeratosis Congenita , Mutation, Missense , Telomerase , Humans , Dermatologists , Dyskeratosis Congenita/genetics , Dyskeratosis Congenita/diagnosis , Skin/pathology , Telomerase/genetics
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