Results 111 to 120 of about 282,297 (205)

Focal palmoplantar keratoderma in 2 children leading to gait abnormalities.

, 2006
Hereditary focal palmoplantar keratoderma are a heterogeneous group of disorders of keratinization characterized by focal areas of thickening of the palms and soles Different genetic abnormalities have been identified for the disorders under this group ...
Adebola. O., Ademola S.A.
core  

A Case Report of Transgrediant Palmoplantar Keratoderma (Mal de Meleda) [PDF]

, 2015
: Mal de Meleda is a rare autosomal recessive transgredient keratoderma .Onset is in early childhood, and the development of hyperkeratosis is preceded by erythema. Patches of waxy ivory-yellow hyperkeratosis extend across the whole palms and soles, and
Darvish Damavandi F., Daraei Z., Shamsadini S.A.,
core  

Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing

European Journal of Dermatology, 2021
So Takeuchi, Takuya Takeichi, Yasutoshi Ito, Kana Tanahashi, Yoshinao Muro, Tomoo Ogi, Masashi Akiyama   +6 more
openaire   +2 more sources

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations. [PDF]

J Med Cases
Alqahtani JM.
europepmc   +1 more source

Palmoplantar Keratoderma: A Mechanism-Based Disease Classification. [PDF]

Clin Cosmet Investig Dermatol
Liu JW, Habulieti X, Qian YT, Ma X, Han Y, Ma DL.   +5 more
europepmc   +1 more source

Arsenical keratoses with Bowen disease in Kuwait revealing transnational household well-water exposure. [PDF]

JAAD Case Rep
Boalbanat H, Alsarraf A, Hassan D, Hasan M.   +3 more
europepmc   +1 more source

Aggressive Periodontitis and Palmoplantar Keratoderma: Papillon-Lefèvre Syndrome in an 11-Year-Old Nepalese Girl. [PDF]

Clin Case Rep
Bhattarai J, Pokhrel S, Poudel Y, Rimal U.   +3 more
europepmc   +1 more source

Punctate Palmoplantar Keratoderma Type 1 (PPPK1) Associated with Pancreatic Intraductal Papillary Mucinous Neoplasm (IPMN): A Case Report. [PDF]

Clin Cosmet Investig Dermatol
AlGarzai RM, Almuhaish LA, Aljarri SA.
europepmc   +1 more source

Integrated bioinformatics analysis reveals convergent molecular signatures associated with SERPINB7 and SERPINA12 deficiency. [PDF]

Front Med (Lausanne)
Xiao Z, Kang Y, Zhao Z, Zeng Y, Zhuo Y, Wang F, Li R, Tan Y.   +7 more
europepmc   +1 more source

Genetic palmoplantar keratoderma associated with <i>SERPINA12</i> mutations. [PDF]

CMAJ
Pan L, Bu Z.
europepmc   +1 more source