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About 279 results

ALLMedicine™ Degos Disease Center

Research & Reviews  139 results

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 References; 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...

Degos disease: a case report and review of the literature.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7594340
Journal of Medical Case Reports; Tummidi S, Nagendran P et. al.

Oct 29th, 2020 - Degos disease is a very rare syndrome with multisystem vasculopathy of unknown cause. It can affect the skin, gastrointestinal tract, and central nervous system. However, other organs such as the kidney, lungs, pleura, and liver can also be involv...

A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis ...
https://doi.org/10.1111/ijd.15092
International Journal of Dermatology REFERENCES; García-Gil MF, Monte Serrano J et. al.

Aug 5th, 2020 - A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis suppurativa.|2020|García-Gil MF,Monte Serrano J,Ramirez-Lluch M,Valero Torres A,López-Giménez MT,|

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Clinicaltrials.gov  139 results

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 References; 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...

Degos disease: a case report and review of the literature.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7594340
Journal of Medical Case Reports; Tummidi S, Nagendran P et. al.

Oct 29th, 2020 - Degos disease is a very rare syndrome with multisystem vasculopathy of unknown cause. It can affect the skin, gastrointestinal tract, and central nervous system. However, other organs such as the kidney, lungs, pleura, and liver can also be involv...

A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis ...
https://doi.org/10.1111/ijd.15092
International Journal of Dermatology REFERENCES; García-Gil MF, Monte Serrano J et. al.

Aug 5th, 2020 - A novel mutation in POFUT1 gene associated with Dowling-Degos disease and hidradenitis suppurativa.|2020|García-Gil MF,Monte Serrano J,Ramirez-Lluch M,Valero Torres A,López-Giménez MT,|

see more →