Results 91 to 100 of about 14,871 (251)
Basal Cell Carcinoma in Type 2 Segmental Darier's Disease
Journal of Skin Cancer, 2012 Background. Darier's disease (DD), also known as Keratosis Follicularis or Darier-White disease, is a rare disorder of keratinization. DD can present as a generalized autosomal dominant condition as well as a localized or segmental postzygotic condition (
Lynne Robertson, Maxwell B. Sauder
doaj +1 more source
Skeletal Class III phenotype: Link between animal models and human genetics: A scoping review
Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, Volume 342, Issue 1, Page 21-44, January 2024.Genetic variants associated with skeletal Class III malocclusion identified in animal models. Identified variants emphasize the role of BMP and TGF‐β signaling in bone growth and ossification regulation. Abstract This study aimed to identify evidence from animal studies examining genetic variants underlying maxillomandibular discrepancies resulting in ...
Alexandra Dehesa‐Santos +2 more
wiley +1 more source
A Case of Familial Comedonal Darier's Disease [PDF]
, 2011 Darier's disease is a genetic disorder of keratinization with autosomal dominant inheritance. Its appearance is usually in the form of greasy, crusted, keratotic yellow-brown papules and plaques found particularly on seborrheic areas of the body. However,
Aliağaoğlu +19 more
core +2 more sources
Comorbidities and Treatment Options for Acne Keloidalis Nuchae
Dermatologic Therapy, Volume 2024, Issue 1, 2024.Acne keloidalis nuchae (AKN) is a condition that involves chronic inflammation of the hair follicles on the occipital scalp and posterior neck that often progresses to keloid‐like plaques. AKN has most commonly been reported to affect postpubertal males of African descent.
Kimberly Smart +3 more
wiley +1 more source
Contribuição ao estudo das doenças hereditárias
Memorias do Instituto Oswaldo Cruz, 1945 Em revisão de conhecimentos sobre doenças hereditárias foi verificada em várias dessas heredopatias (anemia de hemátias em alvo, icterícia hemolítica heredo-familiar. anemia ovalocítica, anemia perniciosa de BIERMER, trombopatia constitucional, distrofia
Ernani Martins da Silva
doaj +1 more source
Dermoscopy as a Noninvasive Diagnostic Tool for Hailey-Hailey Disease and Darier Disease
Dermatology and Therapy, 2023 Introduction Hailey-Hailey disease (HHD) and Darier disease (DD) are rare genetic disorders for which differential diagnosis, especially in less obvious cases, can be difficult.
Marta Kurzeja +5 more
doaj +1 more source
Expanding the Interface: Overlooked Dermatologic Disorders With Ocular Involvement
JEADV Clinical Practice, Volume 4, Issue 5, Page 1239-1243, December 2025.
A George
wiley +1 more source
Jadassohn-Lewandowsky syndrome. Report of the first pediatric case in Cuba
Medisur, 2023 Jadassohn-Lewandowsky syndrome or congenital pachyonychia type 1 belongs to the rare diseases’ group. Worldwide, less than a thousand cases have been described to date and the one that is now published constitutes the first pediatric age report in Cuba ...
Migdalis Hidalgo Muñiz +3 more
doaj
Darier disease : case report with oral manifestations [PDF]
, 2006 Darier disease, also known as keratosis follicularis or dyskeratosis follicularis, is a rare autosomal dominant genodermatosis. It is clinically manifested by hyperkeratotic papules primarily affecting seborrheic areas on the head, neck and thorax ...
Cardoso, Camila Lopes +3 more
core
Keratosis Follicularis Spinulosa Decalvans: A New Observation
, 2017 Scarring alopecia in association with follicular hyperkeratosis is the primary characteristic of keratosis pilaris atrophicans (KPA). It affects mainly the face and scalp and can be inflammatory in nature [1]. Widespread KP can also be seen.
H. Elmahi +4 more
semanticscholar +1 more source