Kosmix
One sec... we're building your guide for
Congenital Ichthyosiform Erythroderma
Congenital ichthyosiform erythroderma
Overview
Treatments
Genetic Information
From Experts
Images
News & Blogs
More
Guides & Articles
Reference
Tools
Health Providers & Organizations
Main ›
Treatments ›
Genetic Information ›
From Experts ›
Images ›
News & Blogs ›
Guides & Articles ›
Reference ›
Tools ›
Health Providers & Organizations ›
Tools
›
Skinsight
Body Location Disease Search
Related in the Kosmos
?
Autosomal recessive disorders
(11)
Eem syndrome
Gerodermia osteodysplastica
Collodion baby
Zunich Kaye syndrome
Meleda Disease
Meleda Disease
Ichthyosis congenita
Netherton syndrome
Kindler syndrome
Bloom syndrome
Neuronal ceroid lipofuscinosis
Multiple sulfatase deficiency
more...
Genetic disorders
(19)
Genodermatoses
Lelis syndrome
Familial cutaneous papillomatosis
Ichthyosis bullosa of siemens
Ichthyosis hystrix
Ichthyosis hystrix
Dermatopathia pigmentosa reticularis
Hay-Wells syndrome
Genetic disease
Pachyonychia congenita
X-linked dominant
Charcot-Marie Tooth Disease
Eem syndrome
Gerodermia osteodysplastica
Collodion baby
Zunich Kaye syndrome
Netherton syndrome
Kindler syndrome
Bloom syndrome
Multiple sulfatase deficiency
more...
Genodermatoses
(157)
Benign familial pemphigus
Bullous congenital ichthyosiform erythroderma
Chondrodysplasia punctata
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
Conradi Hunermann syndrome
Conradi Hunermann syndrome
Epidermolysis bullosa dystrophica
Epidermolysis bullosa simplex
Erythrokeratodermia variabilis
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
Ibids syndrome
Ichthyosis
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
Incontinentia pigmenti
Junctional epidermolysis bullosa (medicine)
Keratosis follicularis spinulosa decalvans
Naegeli syndrome
Neutral lipid storage disease
Peeling skin syndrome
Sjogren-larsson syndrome
X-linked ichthyosis
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
Collodion baby
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
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Familial cutaneous papillomatosis
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
IFAP syndrome
Ichthyosis bullosa of siemens
Ichthyosis congenita
Ichthyosis hystrix
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
Keratosis pilaris
Keratosis pilaris atrophicans faciei
Kindler syndrome
Klinefelter's syndrome
Klippel–Feil syndrome
LEOPARD syndrome
Lelis 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
Meleda Disease
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Netherton 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
Progressive symmetric erythrokeratodermia
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
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
more...
Rare diseases
(20)
Bullous congenital ichthyosiform erythroderma
Lelis syndrome
Eem syndrome
Familial cutaneous papillomatosis
Gerodermia osteodysplastica
Gerodermia osteodysplastica
Collodion baby
Zunich Kaye syndrome
Meleda Disease
Ichthyosis bullosa of siemens
Ichthyosis congenita
Ichthyosis hystrix
Netherton syndrome
Kindler syndrome
Dermatopathia pigmentosa reticularis
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
Neuronal ceroid lipofuscinosis
Multiple sulfatase deficiency
Epidermolysis bullosa simplex
more...
Dermatology
Cutaneous conditions
Keratinocytes
Stratum corneum
Desquamation
Syndromes
(9)
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Sjogren-larsson syndrome
Netherton syndrome
Netherton syndrome
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
Conradi Hunermann syndrome
more...
Papulosquamous hyperkeratotic skin diseases
(57)
Erythroderma
Palmoplantar keratoderma
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
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
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
Keratitisâ- €“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 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...
Keratins
(31)
Keratin
Keratin 1
Keratin 10
Keratin 5
Type II keratin
Type II keratin
Beta-keratin
Cytokeratin
Hair keratin
Keratin 12
Keratin 13
Keratin 14
Keratin 15
Keratin 16
Keratin 17
Keratin 18
Keratin 19
Keratin 20
Keratin 21
Keratin 2A
Keratin 3
Keratin 4
Keratin 6A
Keratin 6B
Keratin 6C
Keratin 7
Keratin 8
Keratin 9
Tonofibril
Type I hair keratin
Type I keratin
Type II hair keratin
more...
Dermatologic terminology
Skin disorder
Genodermatosis
Nevus
Keratosis
Desquamation
Medicine
Diseases and disorders
Cornification
Filaggrin
Gene
NSDHL
SPINK5
ABHD5
ALOX12B
ALOXE3
Keratin 10
Filaggrin
Diseases and disorders
(47)
Netherton syndrome ichthyosis
Eclabium
Ichthyosis hystrix curth macklin type
Ichthyosis male hypogonadism
Bullous erythroderma ichthyosiformis congenita of brocq
Bullous erythroderma ichthyosiformis congenita of brocq
ICE syndrome
Cutis laxa
Cutaneous conditions
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
Ichthyosis
Eem syndrome
Gerodermia osteodysplastica
Collodion baby
Zunich Kaye syndrome
Meleda Disease
Sjogren-larsson syndrome
X-linked ichthyosis
Ichthyosis congenita
Erythroderma
Ichthyosis linearis circumflexa
Netherton syndrome
Dermatopathia pigmentosa reticularis
Neutral lipid storage disease
Ibids syndrome
Acquired ichthyosis
Ichthyosis vulgaris
Hay-Wells syndrome
Benign familial pemphigus
Skin disorder
Naegeli syndrome
Genodermatosis
Bloom syndrome
Epidermolysis bullosa dystrophica
Nevus
Focal dermal hypoplasia
Peeling skin syndrome
Keratosis
Chondrodysplasia punctata
Neuronal ceroid lipofuscinosis
Palmoplantar keratoderma
Keratosis follicularis spinulosa decalvans
Multiple sulfatase deficiency
Epidermolysis bullosa simplex
Incontinentia pigmenti
Charcot-Marie Tooth Disease
Hypohidrotic ectodermal dysplasia
Mental retardation
more...
See also
(20)
Nevus flammeus nuchae
Integument
Subcutaneous tissue
Fatty aldehyde dehydrogenase
ALOX12B
ALOX12B
Gene
ALOXE3
Congenital malformations
Autosomal recessive
TGM1
Fat restriction
Autosomal dominant
Collodion
Epidermis (skin)
Acquired ichthyosis
Central American Integration System
Cadherin
Ipsilateral
Lipoxygenase
Spasticity
more...
more categories...
Health Providers & Organizations
›
Vitals.com
