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Longer titles found: Keratoderma blennorrhagicum (view), Keratoderma climactericum (view), Palmoplantar keratoderma (view), Paraneoplastic keratoderma (view), Drug-induced keratoderma (view), Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome (view), Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome (view), Striate keratoderma (view), Acral keratoderma (view), Skin fragility-woolly hair-palmoplantar keratoderma syndrome (view), Palmoplantar keratoderma with deafness (view)

searching for Keratoderma 41 found (112 total)

alternate case: keratoderma

Keratin 9 (1,030 words) [view diff] exact match in snippet view article find links to article

Mutations in the gene encoding this protein cause epidermolytic palmoplantar keratoderma. GRCh38: Ensembl release 89: ENSG00000171403 – Ensembl, May 2017 GRCm38:

Leukoencephalopathy (231 words) [view diff] no match in snippet view article find links to article

Leukoencephalopathy (leukodystrophy-like diseases) is a term that describes all of the brain white matter diseases, whether their molecular cause is known

Keratin 16 (1,088 words) [view diff] exact match in snippet view article find links to article

disorders including pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus. GRCh38: Ensembl release

List of diseases (K) (406 words) [view diff] exact match in snippet view article

Keratoconus Keratoderma hypotrichosis leukonychia Keratoderma palmoplantar deafness Keratoderma palmoplantar spastic paralysis Keratoderma palmoplantaris

Keratin 6C (658 words) [view diff] exact match in snippet view article find links to article

been identified as being able to cause diffuse and focal palmoplantar keratodermas. This has been identified as a form of Pachyonychia congenita. GRCh38:

List of genes mutated in cutaneous conditions (108 words) [view diff] exact match in snippet view article find links to article

nonepidermolytic palmoplantar keratoderma (Unna–Thost keratoderma) Diffuse epidermolytic palmoplantar keratoderma (Vörner keratoderma) KRT2 Ichthyosis bullosa

Inherited disorders of trafficking (359 words) [view diff] exact match in snippet view article find links to article

1975. CEDNIK syndrome (Cerebral Dysgenesis, Neuropathy, Ichthyosis and Keratoderma Syndrome) is a rare inherited genetic skin condition (Genodermatosis)

Desmoglein-1 (1,595 words) [view diff] exact match in snippet view article find links to article

gene can cause the autosomal dominant mutation striate palmoplantar keratoderma. In 2013, cases have arisen where the homozygous loss of the desmoglein-1

Pancreatic elastase (1,794 words) [view diff] exact match in snippet view article find links to article

suspected to be associated with diffuse nonepidermolytic palmoplantar keratoderma (diffuse NEPPK). However the suspected sequence variant was fully functional

Loricrin (943 words) [view diff] exact match in snippet view article find links to article

basis of loricrin keratodermas". Histol. Histopathol. 13 (3): 819–26. PMID 9690138. Ishida-Yamamoto A (2003). "Loricrin keratoderma: a novel disease entity

Woolly hair autosomal recessive (205 words) [view diff] exact match in snippet view article find links to article

tapered ends. Cardiofaciocutaneous syndrome Naxos disease Palmoplantar keratoderma and cardiomyopathy syndrome There is no treatment for this condition

Knuckle pads (1,301 words) [view diff] exact match in snippet view article find links to article

Acrokeratoelastoidosis of Costa, camptodactyly, epidermolytic palmoplantar keratoderma, Dupuytren's disease, plantar fibromatosis (Ledderhose's disease), and

List of MeSH codes (C17) (3,128 words) [view diff] exact match in snippet view article

Sjögren–Larsson syndrome MeSH C17.800.428.435 – keratoderma, palmoplantar MeSH C17.800.428.435.440 – keratoderma, palmoplantar, diffuse MeSH C17.800.428.435

Craniosynostosis–anal anomalies–porokeratosis syndrome (56 words) [view diff] exact match in snippet view article find links to article

autosomal recessive fashion. Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean

Lichen nitidus (623 words) [view diff] exact match in snippet view article find links to article

may coalesce into plaques that fissure or “...sometimes a non-specific keratoderma resembling chronic eczema,” or (2) become more widespread, with papules

Progressive symmetric erythrokeratodermia (502 words) [view diff] exact match in snippet view article find links to article

[citation needed] This includes erythrokeratodermia variabilis and loricrin keratoderma Definitive treatment does not exist at the moment. Palliative treatment

Desmosome (1,221 words) [view diff] exact match in snippet view article find links to article

desmosomes. Desmoglein 1 haploinsufficiency leads to striate palmoplantar keratoderma, a disease which causes extreme thickening of the epidermis. Loss of

GJB3 (1,068 words) [view diff] exact match in snippet view article find links to article

Richard G, et al. (2000). "Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family". Eur. J. Hum. Genet. 8 (2):

List of neurological conditions and disorders (1,143 words) [view diff] exact match in snippet view article find links to article

infarcts and leukoencephalopathy Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome Cerebral gigantism Cerebral palsy Cerebral vasculitis Cerebrospinal

SNAP29 (1,112 words) [view diff] exact match in snippet view article find links to article

characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma". Am. J. Hum. Genet. 77 (2): 242–51. doi:10.1086/432556. PMC 1224527

Plakoglobin (4,516 words) [view diff] exact match in snippet view article find links to article

LS, Shou W (March 2012). "Lack of plakoglobin in epidermis leads to keratoderma". The Journal of Biological Chemistry. 287 (13): 10435–10443. doi:10

List of diseases (W) (439 words) [view diff] exact match in snippet view article

hypotrichosis everted lower lip outstanding ears Woolly hair palmoplantar keratoderma cardiac anomalies Woolly hair, congenital Worster-Drought syndrome, various

Keratin 1 (1,260 words) [view diff] exact match in snippet view article find links to article

in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma". The Journal of Investigative Dermatology. 103 (6): 764–769. doi:10

Pili torti (4,435 words) [view diff] exact match in snippet view article find links to article

ectodermal dysplasia, hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome, oculo-dento-digital syndrome, pachyonychia congenita-2, Rapp-Hodgkin

Porokeratotic eccrine ostial and dermal duct nevus (949 words) [view diff] exact match in snippet view article find links to article

nevus comedonicus, linear psoriasis, linear epidermal nevus, spiny keratoderma, congenital unilateral punctate porokeratosis, linear porokeratosis,

List of diseases (T) (852 words) [view diff] exact match in snippet view article

Thoracolaryngopelvic dysplasia Thoracopelvic dysostosis Thost–Unna palmoplantar keratoderma Thrombasthenia Thrombocytopathy asplenia miosis Thrombocytopathy Thrombocytopenia

List of diseases (E) (918 words) [view diff] exact match in snippet view article

Epidermolysis bullosa Epidermolytic hyperkeratosis Epidermolytic palmoplantar keratoderma Vorner type Epididymitis Epilepsia partialis continua Epilepsy Epilepsy

Nikos Protonotarios (751 words) [view diff] exact match in snippet view article find links to article

Ventricular Cardiomyopathy With Diffuse Nonepidermolytic Palmoplantar Keratoderma and Woolly Hair (Naxos Disease) Maps to 17q21". Circulation. 97 (20):

List of diseases (L) (900 words) [view diff] exact match in snippet view article

Leukodystrophy, Sudanophilic Leukodystrophy Leukoencephalopathy palmoplantar keratoderma Leukomalacia Leukomelanoderma mental retardation hypotrichosis Leukoplakia

Itch (3,882 words) [view diff] exact match in snippet view article find links to article

of flaking is associated with this sensation. Punctate palmoplantar keratoderma, a group of disorders characterized by abnormal thickening of the palms

List of diseases (D) (1,155 words) [view diff] exact match in snippet view article

Alport syndrome Diffuse neonatal hemangiomatosis Diffuse palmoplantar keratoderma, Bothnian type Diffuse panbronchiolitis Diffuse parenchymal lung disease

Florid cutaneous papillomatosis (1,332 words) [view diff] exact match in snippet view article find links to article

cutaneous papillomatosis, malignant acanthosis nigrica, palmoplantar keratoderma, and gastric adenocarcinoma" (PDF). Acta Medical Iranica. 37 (1). Archived

Dogue de Bordeaux (2,884 words) [view diff] exact match in snippet view article find links to article

the original on 1 June 2012. Retrieved 5 September 2012. "Naso-plantar keratoderma in the Dogue de Bordeaux: epidemiology, clinical and genetic data" (PDF)

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

sex reversal; 610644; RSPO1 Palmoplantar keratoderma, nonepidermolytic; 600962; KRT16 Palmoplantar keratoderma, nonepidermolytic, focal; 613000; KRT16

Absence of fingerprints-congenital milia syndrome (644 words) [view diff] exact match in snippet view article find links to article

thickened skin throughout the body. Single transversal palmar lines, plantar keratoderma, nail grooving, toe syndactyly and finger camptodactyly have also been

List of diseases (P) (1,908 words) [view diff] exact match in snippet view article

Palmer–Pagon syndrome Palmitoyl-protein thioesterase deficiency Palmoplantar Keratoderma Palmoplantar porokeratosis of Mantoux Palsy cerebral Panayiotopoulos

List of MeSH codes (C16) (6,496 words) [view diff] exact match in snippet view article

incontinentia pigmenti MeSH C16.320.850.475 – keratoderma, palmoplantar MeSH C16.320.850.475.440 – keratoderma, palmoplantar, diffuse MeSH C16.320.850.475

Small interfering RNA (7,300 words) [view diff] exact match in snippet view article find links to article

epidermolysis bullosa simplex (Atkinson et al. 2011), epidermolytic palmoplantar keratoderma (EPPK) (Lyu et al. 2016), and lattice corneal dystrophy type I (LCDI)

Periodontal disease (8,985 words) [view diff] exact match in snippet view article find links to article

Ehlers–Danlos syndrome and Papillon–Lefèvre syndrome (also known as palmoplantar keratoderma) are also risk factors for periodontitis. If left undisturbed, microbial

Rheumatoid arthritis (17,047 words) [view diff] exact match in snippet view article find links to article

with urethritis, conjunctivitis, iritis, painless buccal ulcers, and keratoderma blennorrhagica. Axial spondyloarthritis (including ankylosing spondylitis)

Gluten-sensitive enteropathy–associated conditions (7,562 words) [view diff] exact match in snippet view article find links to article

Bonaci-Nikolić B (2006). "Rothmund-Thomson syndrome. The first case with plantar keratoderma and the second with coeliac disease". Acta Dermatovenerologica Alpina