Results 21 to 30 of about 1,355 (174)

Bilateral systematized epidermolytic verrucous epidermal nevus: A rare entity

open access: yesIndian Journal of Dermatology, 2015
Verrucous epidermal nevi are congenital, noninflammatory cutaneous hamartomas composed of keratinocytes. They follow the lines of Blaschko and show hyperkeratosis without cellular atypia.
Vivek Mishra   +3 more
doaj   +1 more source

Is this 4-year-old female child suffering from a forme fruste of hypomelanosis of Ito?

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Hypomelanosis of ito (HI) is a multisystemic disorder characterized by cutaneous, neurologic disorder, and musculoskeletal disorder. However, there may be isolated cutaneous manifestation, resulting in diagnostic overlap with other hypopigmentary lesions
Ibrahim Aliyu   +2 more
doaj   +1 more source

Linear and whorled nevoid hypermelanosis with hyper IgE syndrome

open access: yesPrzegląd Dermatologiczny, 2015
Introduction . Linear and whorled nevoid hypermelanosis (LWNH) is a disorder of pigmentation characterized by macular hyperpigmentation following the Blaschko lines. Only 50 cases of LWNH have been described so far.
Joanna Sieniawska   +4 more
doaj   +1 more source

Blaschko Linear Enamel Defects - A Marker for Focal Dermal Hypoplasia: Case Report of Focal Dermal Hypoplasia

open access: yesCase Reports in Dermatology, 2015
Focal dermal hypoplasia (FDH) is a rare genetic skin disorder. The inheritance of FDH or Goltz-Gorlin syndrome is X-linked dominant and the disease is associated with a PORCN gene mutation.
Stefan Gysin, Peter Itin
doaj   +1 more source

Atypical Linear Atrophoderma of Moulin Complicated with Elevated Immunoglobulin M: A Case Report

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Chenyu Tang,1 Ping Wang2 1Department of Dermatology, Hangzhou Third People’s Hospital, Zhejiang Chinese Medical University, Hangzhou, People’s Republic of China; 2Department of Dermatology, Hangzhou Third People’s Hospital; Affiliated Hangzhou ...
Tang C, Wang P
doaj  

Congenital lichenoid porokeratosis in a child

open access: yesIndian Journal of Paediatric Dermatology, 2022
Linear porokeratosis is a rare disease that can be congenital or may occur typically during infancy and childhood. It presents clinically as streaks or plaques of reddish-brown papules along the Blaschko lines.
Subhra Dhar   +2 more
doaj   +1 more source

Cutaneous Mosaicism Along Blaschko Lines: A Case Series of Epidermal Verrucous Nevus and Linear Whorled Nevoid Hypermelanosis

open access: yesNepal Journal of Dermatology, Venereology & Leprology
Cutaneous mosaicisms are often seen along Blaschko lines. These lines represent ectodermal cell migration. Lesions derived from epidermal components typically follow Blaschko line patterns.
Ruchitha S   +2 more
doaj   +1 more source

Hyperpigmented lesions with acquired atrophy following Blaschko lines in a patient with diagnosed with localized scleroderma

open access: yesBoletín Médico del Hospital Infantil de México, 2021
Background: Linear atrophoderma of Moulin (LAM) is a dermatosis that affects children and adolescents characterized by hyperpigmented and atrophic linear lesions following Blaschko lines. So far, less than 50 cases have been published. Therefore, it is a
Eduardo Marín-Hernández   +2 more
doaj   +1 more source

Linear atrophoderma of Moulin: case report of a rare disease

open access: yesPigment International
Linear atrophoderma of Moulin is a rare, acquired, mostly unilateral entity often presenting with hyperpigmented and atrophic band-like skin lesions that follow the lines of Blaschko.
Preema Sinha   +3 more
doaj   +1 more source

Lúpus eritematoso crônico discoide nas linhas de Blaschko Linear chronic discoid lupus erythematosus following the lines of Blaschko

open access: yesAnais Brasileiros de Dermatologia, 2011
O lúpus eritematoso crônico discoide linear é manifestação rara da doença lúpica cutânea, em que lesões eritêmato-atrófico-discrômicas dispõem-se nas linhas de Blaschko.
Patricia Erica Christofoletti Daldon   +1 more
doaj   +1 more source

Home - About - Disclaimer - Privacy