Results 11 to 20 of about 171 (84)

Reticulate acropigmentation of Kitamura with café-au-lait macules: a rare case report [PDF]

open access: yesFrontiers in Medicine
Reticulate acropigmentation of Kitamura (RAK) predominantly affects East Asian populations, though isolated cases and familial occurrences have been reported globally. Japanese researchers Kitamura et al. first described this condition in 1943.
Bukuan Gao   +5 more
doaj   +2 more sources

Bioinspired Provisional Matrix Stimulates Regenerative Healing of Diabetic Wounds [PDF]

open access: yesWound Repair and Regeneration, Volume 33, Issue 5, September/October 2025.
ABSTRACT This study tested the hypothesis that diabetic wound treatment with biomimetic pro‐angiogenic, proteolytically and mechanically stable RADA16‐II peptide nanofibers promotes regenerative wound healing via attenuation of inflammation and stimulation of neovascularization. Two full‐thickness excisional dorsal skin wounds were created on 8–10 week
Walker D. Short   +11 more
wiley   +2 more sources

Dermoscopy of Dermatopathia Pigmentosa Reticularis

open access: yesIndian Journal of Dermatology, 2022
Maheshwari, Apoorva   +2 more
openaire   +3 more sources

Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders [PDF]

open access: yesDermatology Research and Practice, Volume 2017, Issue 1, 2017., 2017
Reticulated pigmentation is a unique pigmentary change caused by a heterogeneous group of hereditary and acquired disorders. This pigmentation is characterized by a mottled appearance, with lesions that vary in size and pigmentary content. This review discusses the hereditary group of the reticulated pigmentation disorders, such as dyschromatosis ...
H. Alshaikh   +3 more
wiley   +2 more sources

Naegeli-Franceschetti-Jadassohn syndrome: A rare case

open access: yesIndian Dermatology Online Journal, 2015
Naegeli-Franceschetti-Jadassohn Syndrome (NFJS) is a rare, autosomal dominant inherited form of ectodermal dysplasia, caused by mutation in the KRT14 gene.
Bela J Shah   +3 more
doaj   +2 more sources

The spectrum of melanocytic nevi and their clinical implications

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 20, Issue 4, Page 483-504, April 2022., 2022
Summary The magnitude of the topic of melanocytic nevi (MN) is directly related to its relevance in everyday clinical work. The different MN have different prognostic significance in regard to comorbidity and possible risk of transformation. In addition to the criteria of the ABCDE rule, relevant criteria in the assessment of an MN are the time of ...
Nina Frischhut   +3 more
wiley   +1 more source

Das Spektrum melanozytärer Nävi und deren klinische Bedeutung

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 20, Issue 4, Page 483-506, April 2022., 2022
Zusammenfassung Die Größe der Thematik melanozytärer Nävi (MN) steht in einem direkten Verhältnis zur Relevanz in der alltäglichen klinischen Arbeit. Die klinische Präsentation ist hochgradig variabel und verschiedene MN haben unterschiedliche prognostische Bedeutung in Bezug auf Komorbidität und mögliches Entartungsrisiko.
Nina Frischhut   +3 more
wiley   +1 more source

Dermatopathia pigmentosa reticularis

open access: yesIndian Journal of Paediatric Dermatology, 2018
Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Gauri Vats   +3 more
doaj   +1 more source

Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome

open access: yes, 2020
British Journal of Dermatology, Volume 183, Issue 4, Page 756-757, October 2020.
D.J. Ralser   +9 more
wiley   +1 more source

Mucosal and skin pigmentation with abnormal nails

open access: yes
JEADV Clinical Practice, Volume 3, Issue 2, Page 779-781, June 2024.
Fengming Chen, Ling Liu, Pingshen Fan
wiley   +1 more source

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