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About 287 results

ALLMedicine™ Degos Disease Center

Research & Reviews  143 results

Clinical Manifestations and Treatment Outcomes in Degos Disease: A Systematic Review.
https://doi.org/10.1111/jdv.17311
Journal of the European Academy of Dermatology and Venere... Kim PJ, Lytvyn Y et. al.

Apr 29th, 2021 - Degos disease (atrophic papulosis) is a rare vasculopathy with cutaneous and systemic manifestations. Although potentially fatal, the characteristics of and treatments for Degos disease variants are not adequately described. We conducted a systema...

Dowling-Degos disease: a review.
https://doi.org/10.1111/ijd.15385
International Journal of Dermatology References; Stephan C, Kurban M et. al.

Dec 28th, 2020 - Dowling-Degos disease is a rare autosomal dominant genodermatosis. It is characterized by acquired reticulate hyperpigmentation over the flexures, comedone-like follicular papules, and pitted perioral scars that usually develop during adulthood. M...

Degos-like lesions as a cutaneous manifestation of cytomegalovirus infection: A rare an...
https://doi.org/10.1111/1346-8138.15717
The Journal of Dermatology; Chieosilapatham P, Prinyaroj N et. al.

Dec 11th, 2020 - Cytomegalovirus causes a myriad of clinical features, potentially affecting any organ system, significantly increasing morbidity and even mortality. Vascular endothelial cell infection by cytomegalovirus has been implicated in the development of v...

The deregulation of NOTCH pathway, inflammatory cytokines, and keratinization genes in ...
https://doi.org/10.1002/ajmg.a.61800
American Journal of Medical Genetics. Part A REFERENCES; Cortez Cardoso Penha R, Cortez de Almeida RF et. al.

Nov 17th, 2020 - Dowling-Degos disease (DDD) is a rare autosomal-dominant genodermatosis and it has been associated with hidradenitis suppurativa (HS). Deregulation of NOTCH pathway has been linked to the development of HS in DDD context (DDD-HS). However, molecul...

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Clinicaltrials.gov  143 results

Clinical Manifestations and Treatment Outcomes in Degos Disease: A Systematic Review.
https://doi.org/10.1111/jdv.17311
Journal of the European Academy of Dermatology and Venere... Kim PJ, Lytvyn Y et. al.

Apr 29th, 2021 - Degos disease (atrophic papulosis) is a rare vasculopathy with cutaneous and systemic manifestations. Although potentially fatal, the characteristics of and treatments for Degos disease variants are not adequately described. We conducted a systema...

Dowling-Degos disease: a review.
https://doi.org/10.1111/ijd.15385
International Journal of Dermatology References; Stephan C, Kurban M et. al.

Dec 28th, 2020 - Dowling-Degos disease is a rare autosomal dominant genodermatosis. It is characterized by acquired reticulate hyperpigmentation over the flexures, comedone-like follicular papules, and pitted perioral scars that usually develop during adulthood. M...

Degos-like lesions as a cutaneous manifestation of cytomegalovirus infection: A rare an...
https://doi.org/10.1111/1346-8138.15717
The Journal of Dermatology; Chieosilapatham P, Prinyaroj N et. al.

Dec 11th, 2020 - Cytomegalovirus causes a myriad of clinical features, potentially affecting any organ system, significantly increasing morbidity and even mortality. Vascular endothelial cell infection by cytomegalovirus has been implicated in the development of v...

The deregulation of NOTCH pathway, inflammatory cytokines, and keratinization genes in ...
https://doi.org/10.1002/ajmg.a.61800
American Journal of Medical Genetics. Part A REFERENCES; Cortez Cardoso Penha R, Cortez de Almeida RF et. al.

Nov 17th, 2020 - Dowling-Degos disease (DDD) is a rare autosomal-dominant genodermatosis and it has been associated with hidradenitis suppurativa (HS). Deregulation of NOTCH pathway has been linked to the development of HS in DDD context (DDD-HS). However, molecul...

see more →