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Related in the Kosmos
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Genodermatoses
(157)
Benign familial pemphigus
Bullous Ichthyosis
Child syndrome ichthyosis
Chondrodysplasia punctata
Congenital ichthyosiform erythroderma
Congenital ichthyosiform erythroderma
Conradi Hunermann syndrome
Ectodermal dysplasia
Erythrokeratodermia progressiva symmetrica
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Ibids syndrome
Ichthyosis bullosa of siemens
Ichthyosis congenita
Ichthyosis follicularis
Ichthyosis hystrix
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
Ichthyosis, Netherton syndrome
Keratitis-- ichthyosis-deafness syndrome
Keratosis pilaris
Kindler syndrome
Lamellar ichthyosis
Lelis syndrome
Leopard syndrome
Meleda Disease
Neutral lipid storage disease
Peeling skin syndrome
Sjogren-larsson syndrome
X-linked ichthyosis
Xeroderma pigmentosum
Zunich Kaye syndrome
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Apert syndrome
Aplasia cutis congenita
Arrhythmogenic right ventricular dysplasia
Ataxia telangiectasia
Atrichia with papular lesions
Atrophodermia vermiculata
Autoimmune polyendocr- inopathy–candidiasis–ectodermal dystrophy syndrome
BIDS syndrome
Bart syndrome
Bloom syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
Dermatopathia pigmentosa reticularis
Disseminated superficial actinic porokeratosis
Disseminated superficial porokeratosis
Dominant dystrophic epidermolysis bullosa
Dyschromatosis universalis hereditaria
Dyskeratosis congenita
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa
Epidermolysis bullosa dystrophica
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Focal dermal hypoplasia
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein syndrome
Freeman-Sheldon syndrome
Generalized atrophic benign epidermolysis bullosa
Generalized epidermolysis bullosa simplex
Generalized trichoepithelioma
Hallermann-Streiff syndrome
Hay–Wells syndrome
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
Keratosis pilaris atrophicans faciei
Klinefelter's syndrome
Klippel–Feil syndrome
Lentiginosis
Lenz–Majewski syndrome
Linear Darier disease
Linear and whorled nevoid hypermelanosis
Linear porokeratosis
Localized epidermolysis bullosa simplex
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Naegeli–- Franceschetti–Jadassohn syndrome
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
Noonan syndrome
Odonto–T- richo–Ungual–Digital–Palmar syndrome
PIBI(D)S syndrome
POEMS syndrome
Pachydermo- periostosis
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Papillon–Lefèvre syndrome
Pfeiffer syndrome
Pityriasis rotunda
Plaque-type porokeratosis
Polyostotic fibrous dysplasia
Popliteal pterygium syndrome
Porokeratosis
Porokeratosis palmaris et plantaris disseminata
Progeria
Proteus syndrome
Punctate porokeratosis
Rapp–Hodgkin syndrome
Recessive dystrophic epidermolysis bullosa
Refsum's disease
Relapsing linear acantholytic dermatosis
Restrictive dermopathy
Rhizomelic chondrodysplasia punctata
Rombo syndrome
Rothmund–Thomson syndrome
Scleroatrophic syndrome of Huriez
Tooth and nail syndrome
Transient bullous dermolysis of the newborn
Treacher Collins syndrome
Tricho–r- hino–phalangeal syndrome
Tuberous sclerosis
Turner syndrome
Ulerythema
Ulnar–mammary syndrome
Von Hippel – Lindau disease
Watson syndrome
Werner syndrome
Westerhof syndrome
Wilson–Turner syndrome
Wolf–Hirschhorn syndrome
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Zimmermann–Laband syndrome
more...
Diseases and disorders
(52)
Acquired ichthyosis
Cutaneous conditions
Netherton syndrome ichthyosis
Ichthyosis hystrix curth macklin type
Ichthyosis hystrix gravior
Ichthyosis hystrix gravior
Ichthyosis keratosis follicularis spinulosa decalvans
Iga deficiency
Erythroderma
Imperforate anus
Immune thrombocytopenic purpura
Iliotibial band syndrome
Leiomyoma
IgA nephropathy
Leukemic reticuloen- dotheliosis
Lipoid nephrosis
Lateral epicondylitis
Skin disorder
Letterer-Siwe disease
Mesangial proliferative glomerulonephritis
Legg-perthes disease
Late syphilis
Idiopathic myelofibrosis
Lambert eaton syndrome
Intestinal pseudo-obstruction
Keratosis
Gerodermia osteodysplastica
Eem syndrome
Eclabium
Icterus
Ectropion
Keratitis
Pibids syndrome
Dyskeratosis follicularis
Ichthyosis vulgaris
Lamellar ichthyosis
Ichthyosis congenita
X-linked ichthyosis
Keratitis-- ichthyosis-deafness syndrome
Ichthyosis, Netherton syndrome
Ichthyosis follicularis
Child syndrome ichthyosis
Ichthyosis linearis circumflexa
Neutral lipid storage disease
Meleda Disease
Ibids syndrome
Sjogren-larsson syndrome
Zunich Kaye syndrome
Ectodermal dysplasia
Peeling skin syndrome
Benign familial pemphigus
Xeroderma pigmentosum
Chondrodysplasia punctata
more...
Rare diseases
(17)
Lamellar ichthyosis
Ichthyosis congenita
Ichthyosis hystrix
Bullous Ichthyosis
Ichthyosis, Netherton syndrome
Ichthyosis, Netherton syndrome
Ichthyosis follicularis
Ichthyosis bullosa of siemens
Congenital ichthyosiform erythroderma
Legg-perthes disease
Lambert eaton syndrome
Meleda Disease
Lelis syndrome
Gerodermia osteodysplastica
Familial cutaneous papillomatosis
Eem syndrome
Zunich Kaye syndrome
Kindler syndrome
more...
Autosomal recessive disorders
(10)
Lamellar ichthyosis
Ichthyosis congenita
Ichthyosis, Netherton syndrome
Congenital ichthyosiform erythroderma
Meleda Disease
Meleda Disease
Gerodermia osteodysplastica
Eem syndrome
Zunich Kaye syndrome
Kindler syndrome
Xeroderma pigmentosum
more...
Genetic disorders
(15)
Hereditary disorder
Lamellar ichthyosis
Ichthyosis hystrix
Ichthyosis, Netherton syndrome
Ichthyosis follicularis
Ichthyosis follicularis
Ichthyosis bullosa of siemens
Congenital ichthyosiform erythroderma
Leopard syndrome
Lelis syndrome
Gerodermia osteodysplastica
Familial cutaneous papillomatosis
Eem syndrome
Zunich Kaye syndrome
Keratosis pilaris
Kindler syndrome
more...
Dermatology
Stratum corneum
Xerosis
Desquamation
Cutaneous conditions
Papulosquamous hyperkeratotic skin diseases
(57)
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
Camisa disease
Camisa disease
Cardiofaci- ocutaneous syndrome
Clouston's hidrotic ectodermal dysplasia
Complex keratoderma
Corneodermatosseous syndrome
Darier's disease
Diffuse epidermolytic palmoplantar keratoderma
Diffuse nonepidermolytic palmoplantar keratoderma
Diffuse palmoplantar keratoderma
Digitate dermatosis
Erythroderma
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Florid cutaneous papillomatosis
Focal acral hyperkeratosis
Focal palmoplantar keratoderma
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Howel–Evans syndrome
Junctional epidermolysis bullosa with pyloric atresia
Keratitis-- ichthyosis-deafness syndrome
Keratoderma
Keratoderma blennorrhagica
Keratoderma climactericum
Keratolysis exfoliativa
Keratosis punctata of the palmar creases
Keratosis punctata palmaris et plantaris
Kindler syndrome
Large-plaque parapsoriasis
Meleda Disease
Olmsted syndrome
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Palmoplantar keratoderma
Palmoplantar keratoderma and spastic paraplegia
Palmoplantar keratoderma of Sybert
Papillon–Lefèvre syndrome
Parapsoriasis
Pityriasis rosea
Pityriasis rubra pilaris
Porokeratosis plantaris discreta
Punctate palmoplantar keratoderma
Schöpf–- Schulz–Passarge syndrome
Scleroatrophic syndrome of Huriez
Simple keratoderma
Small-plaque parapsoriasis
Spiny keratoderma
Striate keratoderma
Striate palmoplantar keratoderma
Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy
Syndromic keratoderma
Tyrosinemia type II
Vohwinkel syndrome
more...
Dermatologic terminology
Hyperkeratosis
Bullous
Skin disorder
Keratosis
Xerosis
Desquamation
Medicine
Cornification
Idiopathic
Diseases and disorders
Symptoms
Limited range of motion
Lack of strength
Speech impairment
Scaly skin
Idiopathic hypersomnia
Desquamation
See also
(20)
Impacted tooth
Imodium a-d
Lateral collateral ligament
Ileus
Ovovegetarian
Ovovegetarian
Icterus icterus
ABCA12
Leukemoid reaction
Lactovegetarian
Keratinization
Keratins
Impaction
Langhans giant cell
Livedo reticularis
X-linked recessive
North Wales, PA
Autosomal recessive
Nevus flammeus nuchae
Lamellar
Scale (zoology)
more...
more categories...
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