Results 131 to 140 of about 3,958 (176)
Some of the next articles are maybe not open access.
Hereditary palmoplantar keratoderma with deafness
British Journal of Dermatology, 1996A pedigree showing the uncommon association of palmoplantar keratoderma with sensorineural deafness is described.
D A, Fitzgerald, J L, Verbov
openaire +2 more sources
Palmoplantar keratoderma and associated syndromes
Seminars in Dermatology, 1995This article focuses on the current state of knowledge concerning the characterization and classification of palmoplantar keratoderma and associated syndromes. In addition, therapeutic options are discussed. Exact diagnosis enables dermatologists to give patients accurate genetic counseling and may help to detect underlying defects or proneness to ...
Itin PH, Lautenschlager S
openaire +3 more sources
A Distinct Type of Palmoplantar Keratoderma
Pediatric Dermatology, 2009Abstract: Palmoplantar keratodermas (PPK) are a diverse group of disorders. We report a boy with PPK, grayish‐blue hyperkeratotic lesions on the lips and peri‐oral area, opacities on the lower portions of the corneas, mutilation of his right auricle and many other skin lesions.
Mapar, Mohammad Ali, M, Azarbaik
openaire +2 more sources
Palmoplantar keratoderma with tonotubular keratin
Journal of the American Academy of Dermatology, 1991A 61-year-old man with palmoplantar keratoderma with an unusual tonotubular keratin is reported. The histologic findings, genetic transmission, and clinical course were similar to epidermolytic palmoplantar keratoderma (Voerner type), but keratinocytes ultrastructurally displayed a tonotubular cytoskeleton, which has not been previously described ...
A, Wevers, A, Kuhn, G, Mahrle
openaire +2 more sources
Excision and Grafting of Palmoplantar Keratoderma
Journal of Craniofacial Surgery, 2009Palmoplantar keratodermas may present to the clinician with an extremely broad series of clinical findings. Management has also taken on a wide variety of medical and surgical modalities. The literature seems to provide evidence that optimum management consists of surgical excision with skin grafting.
Aron G, Nusbaum +4 more
openaire +2 more sources
Dermatologica, 2009
In a retrospective study, we reevaluated the biopsies that had been obtained, during the past 11 years, from 26 patients presenting with hereditary palmoplantar keratoderma (PPK). Twelve out of 26 biopsies disclosed the histological features of epidermolytic hyperkeratosis, consistent with the diagnosis of epidermolytic PPK of Vörner.
H, Hamm +3 more
openaire +2 more sources
In a retrospective study, we reevaluated the biopsies that had been obtained, during the past 11 years, from 26 patients presenting with hereditary palmoplantar keratoderma (PPK). Twelve out of 26 biopsies disclosed the histological features of epidermolytic hyperkeratosis, consistent with the diagnosis of epidermolytic PPK of Vörner.
H, Hamm +3 more
openaire +2 more sources
Drugs Associated With the Development of Palmoplantar Keratoderma: A Systematic Review
Journal of Cutaneous Medicine and Surgery, 2021Sara Mirali +2 more
exaly