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Pitted keratolysis (also known as keratolysis plantare sulcatum, [1] keratoma plantare sulcatum, [1] and ringed keratolysis [1]) is a bacterial skin infection of the foot. [2] The infection is characterized by craterlike pits on the sole of the feet and toes, particularly weight-bearing areas.
Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome (also known as "HOPP syndrome" [1]) is a cutaneous condition characterized by a prominent palmoplantar 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.
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]
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
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]
Keratoderma blennorrhagicum is commonly seen as an additional feature of reactive arthritis in almost 15% of male patients. The appearance is usually of a vesico-pustular waxy lesion with a yellow brown colour. These lesions may join to form larger crusty plaques with desquamating edges.
[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 ...