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Punctate palmoplantar keratoderma. Keratosis punctata palmaris et plantaris; Spiny keratoderma; Focal acral hyperkeratosis; Complex keratodermas Diffuse palmoplantar keratoderma. Erythrokeratodermia variabilis; Palmoplantar keratoderma of Sybert; Olmsted syndrome; Naegeli–Franceschetti–Jadassohn syndrome; Focal palmoplantar keratoderma
Corneodermatosseous syndrome is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits. [2]
Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide Keratosis punctata of the palmar ...
Acrokeratoelastoidosis of Costa or Acrokeratoelastoidosis is a hereditary form of marginal keratoderma, and can be defined as a palmoplantar keratoderma. It is distinguished by tiny, firm pearly or warty papules on the sides of the hands and, occasionally, the feet. It is less common than the hereditary type of marginal keratoderma ...
Aquagenic keratoderma, also known as acquired aquagenic palmoplantar keratoderma, [4]: 788 transient reactive papulotranslucent acrokeratoderma, [4] aquagenic syringeal acrokeratoderma, [4] and aquagenic wrinkling of the palms, [2] is a skin condition characterized by the development of white papules on the palms after water exposure.
[6]: 562 [10] Multiple minute digitate hyperkeratosis , a rare cutaneous condition, with about half of cases being familial Focal acral hyperkeratosis (also known as "Acrokeratoelastoidosis lichenoides,") is a late-onset keratoderma , inherited as an autosomal dominant condition, characterized by oval or polygonal crateriform papules developing ...
This is a skin disorder that is rare and inherited. [9] It caused by genetics and is an autosomal recessive trait therefore, in order to be affected and present the disease each parent must be a carrier of the mutated allele and pass it to their kids. [6]
Keratitis–ichthyosis–deafness syndrome (KID syndrome), also known as ichthyosiform erythroderma, corneal involvement, and deafness, presents at birth/infancy and is characterized by progressive corneal opacification, either mild generalized hyperkeratosis or discrete erythematous plaques, and neurosensory deafness.