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Darier's disease (DD) is a rare, genetic skin disorder. It is an autosomal dominant disorder, that is, if one parent has DD, there is a 50% chance than a child will inherit DD. It was first reported by French dermatologist Ferdinand-Jean Darier in 1889.
White is one of the namesakes of Darier–White disease, having discovered it independently of Ferdinand-Jean Darier. [1] [2] He also wrote a book, Dermatitis Venenata, published in 1887. [3] White's Back Bay residence, designed by Peabody & Stearns
The other diseases were a follicular keratosis (Darier-White syndrome), dermatofibrosarcoma (Darier-Ferrand disease), erythema annularis, subcutaneous sarcoidosis (Darier-Roussy sarcoid), and a sign, Darier's sign observed in mastocytosis. From 1909 to 1922, Darier was head of the clinical department at the Hôpital Saint-Louis. [5]
It was first described by Darier in 1916. [ 3 ] [ 4 ] [ 5 ] Many different terms have been used to classify these types of lesions and it is still controversial on what exactly defines EAC. Some of the types include annular erythema (deep and superficial), erythema perstans, erythema gyratum perstans, erythema gyratum repens, darier erythema ...
Polydactylous longitudinal erythronychia has been most commonly associated with Darier's disease [10] and lichen planus [11] but has also occasionally been associated with acantholytic epidermolysis bullosa, [12] no association, [13] graft-versus-host disease, [14] [15] hemiplegia, [16] and systemic amyloidosis. [11]
Darier's disease (Darier–White disease, dyskeratosis follicularis, keratosis follicularis) Linear Darier disease; DeSanctis–Cacchione syndrome; Disseminated superficial actinic porokeratosis; Disseminated superficial porokeratosis; Dolichol kinase deficiency; Dominant dystrophic epidermolysis bullosa; Dyskeratosis congenita (Zinsser–Cole ...
Acantholytic dyskeratotic epidermal nevus is a cutaneous condition identical to the generalized form of Darier's disease. [1]: 849 "Acantholytic dyskeratotic epidermal nevus" is probably the same disorder. [1]: 849
Deafness peripheral neuropathy arterial disease; Deafness progressive cataract autosomal dominant; Deafness skeletal dysplasia lip granuloma; Deafness symphalangism; Deafness v – Deafness x. Deafness vitiligo achalasia; Deafness white hair contractures papillomas; Deafness X-linked, DFN3; Deafness, autosomal dominant nonsyndromic sensorineural