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Medical condition
Simple keratodermas Diffuse palmoplantar keratodermas Diffuse epidermolytic palmoplantar keratoderma Diffuse nonepidermolytic palmoplantar keratoderma mal
Keratoderma
Abnormal thickening of skin in the palms or soles
Palmoplantar keratodermas are a heterogeneous group of skin disorders characterized by abnormal thickening (scleroderma) of the stratum corneum of the
Palmoplantar_keratoderma
Skin lesions associated with reactive arthritis
Keratoderma blennorrhagicum (from kerato- 'keratinized'; derma- 'skin'; blenno- 'mucous' and -rrhagia 'discharge'; also called keratoderma blennorrhagica
Keratoderma_blennorrhagicum
palmoplantar keratoderma areata, palmoplantar keratoderma striata, Wachter keratoderma, Wachters palmoplantar keratoderma) Spiny keratoderma (porokeratosis
List_of_skin_conditions
Inflammatory arthritis triggered by infection elsewhere in the body
well as psoriasis-like skin lesions such as circinate balanitis, and keratoderma blennorrhagicum. Enthesitis can involve the Achilles tendon resulting
Reactive_arthritis
Medical condition
as an autosomal dominant syndrome and characterized by palmoplantar keratoderma, oral precursor lesions particularly on the gums (leukoplakia) and a
Howel–Evans_syndrome
Medical condition
non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy" or "diffuse palmoplantar keratoderma with woolly hair and arrhythmogenic
Naxos_syndrome
Growth of keratin on the skin or mucous membranes
follicular keratosis) seborrheic keratosis, not premalignant Folliculitis Keratoderma Merriam-Webster, Merriam-Webster's Unabridged Dictionary, Merriam-Webster
Keratosis
Medical condition
and transgradiens of Siemens, (also known as "acral keratoderma", "mutilating palmoplantar keratoderma of the Gamborg-Nielsen type", "palmoplantar ectodermal
Meleda_disease
Medical condition
Pachyonychia congenita is often associated with thickened toenails, plantar keratoderma, and plantar pain. Pachyonychia congenita is characterized by a clinical
Pachyonychia_congenita
Medical condition
Skin fragility-woolly hair-palmoplantar keratoderma syndrome is a very rare genetic disorder which is characterized by fragile skin which shows itself
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Skin_fragility-woolly_hair-palmoplantar_keratoderma_syndrome
Medical condition
Paraneoplastic keratoderma is a cutaneous condition characterized by a hornlike skin texture associated with an internal malignancy. Keratoderma List of cutaneous
Paraneoplastic_keratoderma
Long-term fungal medical condition
microscopy and culture. It may appear similar to dermatitis, psoriasis, keratoderma, hyperkeratosis and allergic contact dermatitis. Treatment is with long-term
Two_feet-one_hand_syndrome
Medical condition
thickening keratoderma: Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced
Burn_scar_contracture
Medical condition
Keratoderma climactericum, also known as climacteric keratoderma, Haxthausen's disease, or acquired plantar keratoderma, is a skin condition characterized
Keratoderma_climactericum
Term to describe all brain white-matter diseases
Leukoencephalopathy (leukodystrophy-like diseases) is a term that describes all of the brain white matter diseases, whether their molecular cause is known
Leukoencephalopathy
Topics referred to by the same term
Acral keratoderma may refer to: mal de Meleda Striate palmoplantar keratoderma This disambiguation page lists articles associated with the title Acral
Acral_keratoderma
Medical condition
Palmoplantar keratoderma with deafness, also known as Palmoplantar keratoderma-deafness syndrome is a rare genetic disorder which is characterized by
Palmoplantar keratoderma with deafness
Palmoplantar_keratoderma_with_deafness
Medical condition
Striate keratodermas are a group of autosomal dominant palmoplantar keratodermas with streaking hyperkeratosis involving the fingers and extending onto
Striate_keratoderma
Medical condition
palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. In addition to palmoplantar keratoderma, other symptoms
Schöpf–Schulz–Passarge syndrome
Schöpf–Schulz–Passarge_syndrome
Medical condition
Drug-induced keratoderma is a cutaneous condition characterized by a hornlike skin texture. Keratoderma List of cutaneous conditions Rapini, Ronald P.;
Drug-induced_keratoderma
Hardening of finger or toe skin into a claw-like shape
Sclerodactyly is also one component of Huriez Syndrome, along with palmoplantar keratoderma and skin cancer. Sclerodactyly sometimes arises as a complication of
Sclerodactyly
Medical condition
Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome is a neurocutaneous condition caused by mutation in the SNAP29 gene. CEDNIK syndrome is
CEDNIK_syndrome
Medical condition
Papillon–Lefèvre syndrome (PLS), also known as palmoplantar keratoderma with periodontitis, is an autosomal recessive genetic disorder caused by a deficiency
Papillon–Lefèvre_syndrome
Abnormality in the tissue of an organism
Olney's lesions Skin lesions Melanocytic nevus Skip lesion Osler's node Keratoderma blennorrhagicum Dermatosis papulosa nigra Leukemid Janeway lesion Kaposi's
Lesion
Medical condition
congenita and sclerosing keratoderma syndrome (KLICK syndrome) is a rare cutaneous condition characterized by ichthyosis and keratoderma. It is an autosomal
Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
Keratosis_linearis_with_ichthyosis_congenita_and_sclerosing_keratoderma_syndrome
Rare type of lymphoma
convoluted nuclei) Hepatosplenomegaly– enlarged liver and spleen Palmoplantar keratoderma – thickening of the palms of the hands, and soles of the feet Those who
Sézary_disease
Medical condition
Diffuse epidermolytic palmoplantar keratoderma Diffuse nonepidermolytic palmoplantar keratoderma Palmoplantar keratoderma of Sybert Meleda disease syndromic
Gerodermia_osteodysplastica
nonepidermolytic palmoplantar keratoderma (Unna–Thost keratoderma) Diffuse epidermolytic palmoplantar keratoderma (Vörner keratoderma) KRT2 Ichthyosis bullosa
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Structural fibrous protein
occur in a variety of conditions including keratosis, hyperkeratosis and keratoderma. Mutations in keratin gene expression can lead to, among others: Alopecia
Keratin
Medical condition
keratoderma–periodontitis syndrome (also known as "HOPP syndrome") is a cutaneous condition characterized by a prominent palmoplantar keratoderma. Hereditary
Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar_keratoderma–periodontitis_syndrome
Neuromuscular disease
neuropathies Hereditary motor neuropathies Low copy repeats Palmoplantar keratoderma and spastic paraplegia Szigeti K, Lupski JR (2009). "Charcot–Marie–Tooth
Charcot–Marie–Tooth_disease
Medical condition
name ARVC. ACM can be found in association with diffuse palmoplantar keratoderma, and woolly hair, in an autosomal recessive condition called Naxos disease
Arrhythmogenic_cardiomyopathy
Syndromes
Hypotonia Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome Hypotrichosis–lymphedema–telangiectasia syndrome
List_of_syndromes
Organic compound
for psoriasis, xerosis, onychomycosis, ichthyosis, eczema, keratosis, keratoderma, corns, and calluses. If covered by an occlusive dressing, 40% urea preparations
Urea
Medical condition
Bart–Pumphrey syndrome, also known as palmoplantar keratoderma with knuckle pads and leukonychia and deafness) is a cutaneous condition characterized
Bart–Pumphrey_syndrome
Medical condition
fine scaling (and sparing of face), hyperkeratosis, and palmoplantar keratoderma Peeling skin syndrome 5 is caused by a genetic defect in the serpin (serpin
Peeling_skin_syndrome
Type of autoimmune arthritis
with urethritis, conjunctivitis, iritis, painless buccal ulcers, and keratoderma blennorrhagica. Axial spondyloarthritis (including ankylosing spondylitis)
Rheumatoid_arthritis
Change of the skin that affects its color, appearance, or texture
or spotted fevers, guttate psoriasis, hand, foot and mouth disease, keratoderma blennorrhagicum); Symmetry: e.g., herpes zoster usually only affects
Rash
Genetic skin disease
porphyria, white sponge nevus, ichthyosis, epidermolytic palmoplantar keratoderma, hereditary benign intraepithelial dyskeratosis and so on. The second
Genodermatosis
Protein found in humans
Mutations in the gene encoding this protein cause epidermolytic palmoplantar keratoderma. GRCh38: Ensembl release 89: ENSG00000171403 – Ensembl, May 2017 GRCm38:
Keratin_9
Medical condition
Haim–Munk syndrome (also known as palmoplantar keratoderma with periodontitis and arachnodactyly, acro-osteolysis and Cochin Jewish syndrome) is a skin
Haim–Munk_syndrome
List of histologic stains that aid in diagnosis of cutaneous conditions Keratoderma M, Orne, Charisse; S, Hale, Christopher; A, Meehan, Shane; Marie, Leger
List of cutaneous conditions caused by problems with junctional proteins
List_of_cutaneous_conditions_caused_by_problems_with_junctional_proteins
Medical condition
ketoadipiaciduria, koraxitrachitic syndrome, ichthyosis variegata and palmoplantar keratoderma with anogenital leukokeratosis. Since many of these conditions have an
Lamellar_ichthyosis
Medical condition
palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, brachydactyly, short stature, and medullary narrowing of digits. Palmoplantar keratoderma Keratoderma
Corneodermatoosseous_syndrome
List of histologic stains that aid in diagnosis of cutaneous conditions Keratoderma Bolognia, Jean L.; et al. (2007). Dermatology. St. Louis: Mosby. ISBN 1-4160-2999-0
List of cutaneous conditions caused by mutations in keratins
List_of_cutaneous_conditions_caused_by_mutations_in_keratins
Medical condition
Acrokeratoelastoidosis is a hereditary form of marginal keratoderma, and can be defined as a palmoplantar keratoderma. It is distinguished by tiny, firm pearly or
Acrokeratoelastoidosis of Costa
Acrokeratoelastoidosis_of_Costa
Uncomfortable skin sensation
of flaking is associated with this sensation. Punctate palmoplantar keratoderma, a group of disorders characterized by abnormal thickening of the palms
Itch
Protein found in humans
where it may present with acute myocardial injury; striate palmoplantar keratoderma, Carvajal syndrome and paraneoplastic pemphigus. Desmoplakin exists as
Desmoplakin
Thickening of the outermost layer of skin (stratum corneum) due to keratin accumulation
(also known as "Acrokeratoelastoidosis lichenoides,") is a late-onset keratoderma, inherited as an autosomal dominant condition, characterized by oval
Hyperkeratosis
Keratoconus Keratoderma hypotrichosis leukonychia Keratoderma palmoplantar deafness Keratoderma palmoplantar spastic paralysis Keratoderma palmoplantaris
List_of_diseases_(K)
infarcts and leukoencephalopathy Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome Cerebral gigantism Cerebral palsy Cerebral vasculitis Cerebrospinal
List of neurological conditions and disorders
List_of_neurological_conditions_and_disorders
Disease of the skin of human fingers
Acrokeratoelastoidosis of Costa, camptodactyly, epidermolytic palmoplantar keratoderma, Dupuytren's disease, plantar fibromatosis (Ledderhose's disease), and
Knuckle_pads
Medical condition
skin KRT1, KRT10 Ichthyosis bullosa of Siemens skin KRT2A Palmoplantar keratoderma skin KRT1, KRT9, KRT16 Pachyonychia congenita skin KRT6A, KRT6B, KRT16
Keratin_disease
Dog breed originating in France
the original on 1 June 2012. Retrieved 5 September 2012. "Naso-plantar keratoderma in the Dogue de Bordeaux: epidemiology, clinical and genetic data" (PDF)
Dogue_de_Bordeaux
Protein-coding gene in the species Homo sapiens
basis of loricrin keratodermas". Histol. Histopathol. 13 (3): 819–26. PMID 9690138. Ishida-Yamamoto A (2003). "Loricrin keratoderma: a novel disease entity
Loricrin
Cell junction involved in cell-to-cell adhesion
desmosomes. Desmoglein 1 haploinsufficiency leads to striate palmoplantar keratoderma, a disease which causes extreme thickening of the epidermis. Loss of
Desmosome
Dermatologic drug
skin and rough skin Dermatitis Psoriasis Ichthyosis Eczema Keratosis Keratoderma Corns Calluses Damaged, ingrown and devitalized nails Common side effects
Urea-containing_cream
Medical condition affecting scalp hair
dystrophic, thick, and distally separated from the nail bed. Palmoplantar keratoderma may develop during childhood and increases in severity with age. The
Clouston's hidrotic ectodermal dysplasia
Clouston's_hidrotic_ectodermal_dysplasia
Thoracolaryngopelvic dysplasia Thoracopelvic dysostosis Thost–Unna palmoplantar keratoderma Thrombasthenia Thrombocytopathy asplenia miosis Thrombocytopathy Thrombocytopenia
List_of_diseases_(T)
hypotrichosis everted lower lip outstanding ears Woolly hair palmoplantar keratoderma cardiac anomalies Woolly hair, congenital Worster-Drought syndrome, various
List_of_diseases_(W)
Family of disorders causing dry, thickened, scaly skin
Epidermolytic nevi 113800 Postzygotic mosaicism KRT1, KRT10 Loricrin keratoderma 604117 Autosomal dominant LOR Erythrokeratodermia variabilis 133200 Autosomal
Ichthyosis
X-linked dominant 1:25,000 Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome (CEDNIK) SNAP29 <1:1,000,000 Cleft palate short stature vertebral
List_of_genetic_disorders
Medical condition
loricrin. It was characterized in 1984 and 1988. Palmoplantar keratoderma Keratoderma List of cutaneous conditions Freedberg, et al. (2003). Fitzpatrick's
Camisa_disease
Protein found in humans
disorders including pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus. GRCh38: Ensembl release
Keratin_16
Medical condition
mental disability, enteropathy, deafness, neuropathy, ichthyosis, and keratoderma (MEDNIK). People with MEDNIK syndrome often have a high forehead, upslanting
MEDNIK_syndrome
Medical condition
ectodermal dysplasia, hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome, oculo-dento-digital syndrome, pachyonychia congenita-2, Rapp-Hodgkin
Pili_torti
Disease of the tissues surrounding the teeth (periodontium)
Ehlers–Danlos syndrome and Papillon–Lefèvre syndrome (also known as palmoplantar keratoderma) are also risk factors for periodontitis. If left undisturbed, microbial
Periodontal_disease
Biomolecule
epidermolysis bullosa simplex (Atkinson et al. 2011), epidermolytic palmoplantar keratoderma (EPPK) (Lyu et al. 2016), and lattice corneal dystrophy type I (LCDI)
Small_interfering_RNA
Protein found in humans
gene can cause the autosomal dominant mutation striate palmoplantar keratoderma. In 2013, cases have arisen where the homozygous loss of the desmoglein-1
Desmoglein-1
Protein found in humans
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
Keratin_1
Medical condition
Erythrokeratodermia variabilis (also known as "erythrokeratodermia figurata variabilis", "keratosis extremitatum progrediens", "keratosis palmoplantaris
Erythrokeratodermia variabilis
Erythrokeratodermia_variabilis
Class of enzymes
suspected to be associated with diffuse nonepidermolytic palmoplantar keratoderma (diffuse NEPPK). However the suspected sequence variant was fully functional
Pancreatic_elastase
Medical condition
thickened skin throughout the body. Single transversal palmar lines, plantar keratoderma, nail grooving, toe syndactyly and finger camptodactyly have also been
Absence of fingerprints-congenital milia syndrome
Absence_of_fingerprints-congenital_milia_syndrome
Topics referred to by the same term
founded by Frederick Law Olmsted's two sons Olmsted syndrome, a congenital keratoderma of the palms and soles Olmstead (disambiguation) This disambiguation
Olmsted
Alport syndrome Diffuse neonatal hemangiomatosis Diffuse palmoplantar keratoderma, Bothnian type Diffuse panbronchiolitis Diffuse parenchymal lung disease
List_of_diseases_(D)
Medical condition
follicular plugging, keratosis pilaris, xerosis, eczema, palmoplantar keratoderma, syndactyly, onychodysplasia and conjunctival neovascularization. Skin
Ectodermal dysplasia with corkscrew hairs
Ectodermal_dysplasia_with_corkscrew_hairs
Medical condition
restrictions of phenylalanine and tyrosine.[citation needed] Palmoplantar keratoderma List of cutaneous conditions James WD, Elston DM, Berger TG, Andrews
Tyrosinemia_type_II
Protein-coding gene in the species Homo sapiens
characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma". American Journal of Human Genetics. 77 (2): 242–251. doi:10.1086/432556
SNAP29
Mammalian protein found in Homo sapiens
LS, Shou W (March 2012). "Lack of plakoglobin in epidermis leads to keratoderma". The Journal of Biological Chemistry. 287 (13): 10435–10443. doi:10
Plakoglobin
Subfamily of proteins
desmocollin gene mutations include Carvajal syndrome, striate palmoplantar keratoderma, Naxos disease, and arrhythmogenic right ventricular cardiomyopathy.
Desmocollin
American biologist
hemiplegia of childhood, certain subtypes of epilepsy, palmoplantar keratoderma, and Fanconi anemia. From 2007 to 2009, he was scientific director of
Jared_Roach
sex reversal; 610644; RSPO1 Palmoplantar keratoderma, nonepidermolytic; 600962; KRT16 Palmoplantar keratoderma, nonepidermolytic, focal; 613000; KRT16
List_of_OMIM_disorder_codes
Leukodystrophy, Sudanophilic Leukodystrophy Leukoencephalopathy palmoplantar keratoderma Leukomalacia Leukomelanoderma mental retardation hypotrichosis Leukoplakia
List_of_diseases_(L)
American geneticist (born 1978)
AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma". Nature Genetics. 44 (11): 1272–1276. doi:10.1038/ng.2444. PMC 3836166
Bruno_Reversade
incontinentia pigmenti MeSH C16.320.850.475 – keratoderma, palmoplantar MeSH C16.320.850.475.440 – keratoderma, palmoplantar, diffuse MeSH C16.320.850.475
List_of_MeSH_codes_(C16)
Proteins
disorders, such as epidermolytic hyperkeratosis (EHK) and palmoplantar keratoderma (PPK), which are characterized by hyperkeratosis and blistering of the
Type_II_keratin
Medical condition
nevus comedonicus, linear psoriasis, linear epidermal nevus, spiny keratoderma, congenital unilateral punctate porokeratosis, linear porokeratosis,
Porokeratotic eccrine ostial and dermal duct nevus
Porokeratotic_eccrine_ostial_and_dermal_duct_nevus
Medical condition
autosomal recessive fashion. Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean
Craniosynostosis–anal anomalies–porokeratosis syndrome
Craniosynostosis–anal_anomalies–porokeratosis_syndrome
Medical condition
Keratitis–ichthyosis–deafness syndrome (KID syndrome), also known as ichthyosiform erythroderma, corneal involvement, and deafness, presents at birth/infancy
Keratitis–ichthyosis–deafness syndrome
Keratitis–ichthyosis–deafness_syndrome
Palmer–Pagon syndrome Palmitoyl-protein thioesterase deficiency Palmoplantar Keratoderma Palmoplantar porokeratosis of Mantoux Palsy cerebral Panayiotopoulos
List_of_diseases_(P)
Protein found in humans
been identified as being able to cause diffuse and focal palmoplantar keratodermas. This has been identified as a form of Pachyonychia congenita. GRCh38:
Keratin_6C
Epidermolysis bullosa Epidermolytic hyperkeratosis Epidermolytic palmoplantar keratoderma Vorner type Epididymitis Epilepsia partialis continua Epilepsy Epilepsy
List_of_diseases_(E)
Greek researcher and cardiologist
Ventricular Cardiomyopathy With Diffuse Nonepidermolytic Palmoplantar Keratoderma and Woolly Hair (Naxos Disease) Maps to 17q21". Circulation. 97 (20):
Nikos_Protonotarios
Protein-coding gene in the species Homo sapiens
disorder, keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK) syndrome. GRCh38: Ensembl release 89: ENSG00000132963 – Ensembl
POMP
Medical condition
periungal cuticles, corneal dystrophy with photophobia, and palmoplantar keratoderma. The aberrant keratinization of the follicular infundibulum causes keratosis
Keratosis_pilaris_atrophicans
Medical conditions
Bonaci-Nikolić B (2006). "Rothmund-Thomson syndrome. The first case with plantar keratoderma and the second with coeliac disease". Acta Dermatovenerologica Alpina
Gluten-sensitive enteropathy–associated conditions
Gluten-sensitive_enteropathy–associated_conditions
Reddening, swelling, numbness and skin peeling due to chemotherapy
chemotherapy. Long-term chemotherapy may also result in reversible palmoplantar keratoderma. Symptoms resolve 1–2 weeks after cessation of chemotherapy. The range
Chemotherapy-induced acral erythema
Chemotherapy-induced_acral_erythema
Medical condition
in skin pigmentation patterns as well as the presence of palmoplantar keratoderma with yellow tinting of the skin can indicate a possible case of DPR.
Dermatopathia pigmentosa reticularis
Dermatopathia_pigmentosa_reticularis
Topics referred to by the same term
Tylosis may refer to: In medicine Diffuse nonepidermolytic palmoplantar keratoderma, a skin condition of the palms and soles Howel–Evans syndrome, a skin
Tylosis
KERATODERMA
KERATODERMA
KERATODERMA
KERATODERMA
Boy/Male
Hindu, Indian, Marathi
A Sage
Boy/Male
Biblical
Armed with a dart.
Girl/Female
Tamil
Rain, Love
Girl/Female
Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit
Melodious; Sweet
Boy/Male
American, Australian, British, Chinese, Christian, Danish, Dutch, English, Finnish, French, German, Greek, Indian, Irish, Jamaican, Latin, Marathi, Polish, Portuguese, Swedish, Swiss
To Wear a Crown; Wreath; Garland; Crowned
Boy/Male
Gujarati, Hindu, Indian
King of Earth; King of Land
Girl/Female
Norse
Goddess of the underworld.
Boy/Male
Scottish
Son of Henry.
Girl/Female
Hindu
Prayer, Request, Humility
Boy/Male
British, Danish, English, Finnish, Hebrew, Latin
Descend; Farmer; Flowing Down
KERATODERMA
KERATODERMA
KERATODERMA
KERATODERMA
KERATODERMA