keratoderma การใช้

• Mutations in the gene encoding this protein cause epidermolytic palmoplantar keratoderma.
• Mutations in K6C have been identified as being able to cause diffuse and focal palmoplantar keratodermas.
• Keratoderma blennorrhagicum is commonly seen as an additional feature of reactive arthritis in almost 15 % of male patients.
• Note that gangrene, amputation and palmoplantar keratoderma are illustrated on-page, however, which I support.
• Patients can also present with mucocutaneous lesions, as well as psoriasis-like skin lesions such as circinate balanitis, and keratoderma blennorrhagicum.
• Mutations in the gene encoding this protein are associated with the genetic skin disorders pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus.
• Pachyonychia congenita type 2, an autosomal dominant inherited disorder, is characterized by hypertrophic nail dystrophy, focal keratoderma, multiple pilosebaceous cysts, and a variety of conditions associated with ectodermal dysplasia.
• Less well documented causes include Sj鰃ren-Larsson syndrome, Netherton syndrome, Gaucher disease type 2, congenital hypothyroidism, Conradi syndrome, Dorfman-Chanarin syndrome, ketoadipiaciduria, koraxitrachitic syndrome, ichthyosis variegata and palmoplantar keratoderma with anogenital leukokeratosis.
• ARVD can be found in association with diffuse palmoplantar keratoderma, and woolly hair, in an autosomal recessive condition called Naxos disease, because this genetic abnormality can also affect the integrity of the superficial layers of the skin most exposed to pressure stress.
• This condition is inherited as an autosomal dominant syndrome and characterized by palmoplantar keratoderma, oral precursor lesions particularly on the gums ( leukoplakia ) and a high lifetime risk of esophageal cancer ( 95 % develop esophageal cancer by the age of 65 ).
• CEDNIK syndrome ( Cerebral Dysgenesis, Neuropathy, Ichthyosis and Keratoderma Syndrome ) is a rare inherited genetic skin condition ( Genodermatosis ) which has been associated with a loss-of-function mutation in SNAP29; SNAP29 is a member of the SNAP Receptor ( SNARE ) protein family.
• :: Hair growth on the foot sole is possible by deliberate Hair transplantation or by a rare skin disorder Palmoplantar keratoderma-see Carvajal syndrome " Striate palmoplantar keratoderma with woolly hair and cardiomyopathy " with references cited in the article . talk ) 10 : 55, 19 September 2015 ( UTC)
• :: Hair growth on the foot sole is possible by deliberate Hair transplantation or by a rare skin disorder Palmoplantar keratoderma-see Carvajal syndrome " Striate palmoplantar keratoderma with woolly hair and cardiomyopathy " with references cited in the article . talk ) 10 : 55, 19 September 2015 ( UTC)
• "' Clouston's hidrotic ectodermal dysplasia "'( also known as " Alopecia congenita with keratosis palmoplantaris, " " Clouston syndrome, " " Fischer Jacobsen Clouston syndrome, " " Hidrotic ectodermal dysplasia, " " Keratosis palmaris with drumstick fingers, " and " Palmoplantar keratoderma and clubbing " ) is caused by mutations in a connexin gene, GJB6 or connexin-30, characterized by scalp hair that is wiry, brittle, and pale, often associated with patchy alopecia.
• "' Meleda disease "'( MDM ) or " "'mal de Meleda "'", also called "'Mljet disease "', "'keratosis palmoplantaris "'and "'transgradiens of siemens "', ( also known as " Acral keratoderma, " and " Palmoplantar keratoderma of the Norrbotten type " ) is an extremely rare autosomal recessive congenital skin disorder in which dry, thick patches of skin develop on the soles of the hands and feet, a condition known as palmoplantar hyperkeratosis.
• "' Meleda disease "'( MDM ) or " "'mal de Meleda "'", also called "'Mljet disease "', "'keratosis palmoplantaris "'and "'transgradiens of siemens "', ( also known as " Acral keratoderma, " and " Palmoplantar keratoderma of the Norrbotten type " ) is an extremely rare autosomal recessive congenital skin disorder in which dry, thick patches of skin develop on the soles of the hands and feet, a condition known as palmoplantar hyperkeratosis.