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.
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:: 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)
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:: 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)
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"' 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.
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"' 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.
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"' 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.
