Zobrazeno 1 - 10
of 90
pro vyhledávání: '"reticulate hyperpigmentation"'
Publikováno v:
Journal of the Egyptian Women’s Dermatologic Society, Vol 17, Iss 1, Pp 57-61 (2020)
Riehl’s melanosis is a rare case of pigmented contact dermatitis on the face that is characterized by hyperpigmented patches secondary to dermal melanin deposits. The clinical manifestations may vary in pattern and color of hyperpigmentation. The m
Externí odkaz:
https://doaj.org/article/1a79ec9ea93d4e00bb36878ef3a5458e
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 6, Pp 403-406 (2015)
Naegeli-Franceschetti-Jadassohn Syndrome (NFJS) is a rare, autosomal dominant inherited form of ectodermal dysplasia, caused by mutation in the KRT14 gene. We report here a case of NFJS in a 27-year-old male who presented with reticulate hyperpigment
Externí odkaz:
https://doaj.org/article/77d0e51a291a4561aa3e10ca3eefad5d
Publikováno v:
Indian Dermatology Online Journal, Vol 7, Iss 4, Pp 275-277 (2016)
Dyskeratosiscongenita (DKC) is a genetically heterogeneous disease of defective telomere maintenance that may demonstrate different patterns of inheritance. It is characterized by thetriad of dystrophy of the nails, leukokeratosis of the oral mucosa,
Externí odkaz:
https://doaj.org/article/ddcb49ffe8ed4dcf8d66709d32c1ef7f
Publikováno v:
JAAD Case Reports
Dermatopathia pigmentosa reticularis (DPR) is an extremely rare autosomal dominant ectodermal dysplasia that occurs because of mutations in KRT14. It mainly affects the skin, nails, and hair, with a characteristic diagnostic triad of widespread retic
Autor:
Manahel Mahmood AlSabbagh
Publikováno v:
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 18:943-967
Dyskeratosis congenita is a rare hereditary disease that occurs predominantly in males and manifests clinically as the classic triad of reticulate hyperpigmentation, nail dystrophy and leukoplakia. It increases the risk of malignancy and other potent
Publikováno v:
Oxford Medical Case Reports
Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia and onychodystrophy. We report the first case from Syria with classical features of the triad
Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 64, Iss 2, Pp 149-151 (2019)
Indian Journal of Dermatology, Vol 64, Iss 2, Pp 149-151 (2019)
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia that presents with a triad of reticulate hyperpigmentation, nonscarring alopecia, and nail dystrophy. We report herein a case of a 23-year-old male presenting with the characteristic
Autor:
Serena Gianfaldoni, Georgi Tchernev, Torello Lotti, Jacopo Lotti, Uwe Wollina, Roberto Gianfaldoni
Publikováno v:
Open Access Macedonian Journal of Medical Sciences
BASE-Bielefeld Academic Search Engine
Open Access Macedonian Journal of Medical Sciences; Vol 5, No 4 (2017): Jul 25 (OAMJMS) Global Dermatology-1; 432-435
Open Access Macedonian Journal of Medical Sciences; Vol 5 No 4 (2017): Jul 25 (OAMJMS) Global Dermatology-1; 432-435
Open Access Macedonian Journal of Medical Sciences, Vol 5, Iss 4, Pp 432-435 (2017)
BASE-Bielefeld Academic Search Engine
Open Access Macedonian Journal of Medical Sciences; Vol 5, No 4 (2017): Jul 25 (OAMJMS) Global Dermatology-1; 432-435
Open Access Macedonian Journal of Medical Sciences; Vol 5 No 4 (2017): Jul 25 (OAMJMS) Global Dermatology-1; 432-435
Open Access Macedonian Journal of Medical Sciences, Vol 5, Iss 4, Pp 432-435 (2017)
Erythema ab igne is a localised, cutaneous condition consisting of reticulate hyperpigmentation, epidermal atrophy, and telangiectasias. It is caused by repetitive and prolonged exposure to moderate heat that is insufficient for producing burns. Curr
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 19, Iss 1, Pp 77-79 (2018)
Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. A 12-year-old Indian boy presented with classical features of the triad
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