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Cutis Laxa
Cutis laxa
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Related in the Kosmos
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Abnormalities of dermal fibrous and elastic tissue
(18)
Acrodermatitis Chronica Atrophicans
Blepharochalasis
Ehlers Danlos Syndrome
Gerodermia osteodysplastica
Marfan syndrome
Marfan syndrome
Osteogenesis imperfecta
Pseudoxanthoma elasticum
Wrinkly skin syndrome
Anetoderma
Elastosis perforans serpiginosa
Homocystinuria
Linear focal elastosis
Perforating calcific elastosis
Reactive perforating collagenosis
Stretch marks
Striae distensae
Ullrich disease
Verrucous perforating collagenoma
more...
Diseases and disorders
(54)
Cutis laxa recessive
Syndromes
Eem syndrome
Zunich Kaye syndrome
Occipital horn syndrome
Occipital horn syndrome
Meleda Disease
Ichthyosis lamellaris
De barsy syndrome
Congenital hypomyelination
Dermatopathia pigmentosa reticularis
Camptomelic syndrome
Connective tissue diseases
Microphthalmia cataract
Chromosome 9 trisomy
Chromosome 9 tetrasomy 9p
Chromosome 5 trisomy 5p
Epidermolysis bullosa dystrophica
Dermatochalasis
Progeria
Naegeli syndrome
Bloom syndrome
Hay-Wells syndrome
Harlequin type ichthyosis
Acquired ichthyosis
Ectropion
Craniofacial dysostosis
Xeroderma pigmentosum
Menkes disease
Craniosynostosis
Amyloidosis
Focal dermal hypoplasia
Congenital disorder of glycosylation
Epidermolysis bullosa simplex
Rare diseases
Dermatoses
Erythema multiforme
X-linked ichthyosis
Netherton syndrome
Partial monosomy
Charcot marie tooth
Hypohidrotic ectodermal dysplasia
Connective tissue disorder
Cystinosis
Acanthosis nigricans
Mental retardation
Charge syndrome
Costello syndrome
Visceroptosis
Gerodermia osteodysplastica
Ehlers Danlos Syndrome
Wrinkly skin syndrome
Osteogenesis imperfecta
Pseudoxanthoma elasticum
Marfan syndrome
more...
Syndromes
(13)
Lelis syndrome
Hypermobility
Williams syndrome
Eem syndrome
Zunich Kaye syndrome
Zunich Kaye syndrome
Ehlers Danlos Syndrome
Naegeli syndrome
Marfan syndrome
Bloom syndrome
Hay-Wells syndrome
Craniofacial dysostosis
Netherton syndrome
Charge syndrome
more...
Papulosquamous hyperkeratotic skin diseases
Familial cutaneous papillomatosis
Kindler syndrome
Meleda Disease
Cutaneous conditions
(8)
Acral Acanthotic Anomaly
Acne aestivalis
Papulosquamous hyperkeratotic skin diseases
Connective tissue diseases
Wrinkly skin syndrome
Wrinkly skin syndrome
Acquired ichthyosis
Dermatoses
Erythema multiforme
more...
Autosomal recessive disorders
(13)
Congenital ichthyosiform erythroderma
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Meleda Disease
Ichthyosis lamellaris
Kindler syndrome
Pseudoxanthoma elasticum
Bloom syndrome
Harlequin type ichthyosis
Xeroderma pigmentosum
Netherton syndrome
Cystinosis
more...
Congenital disorders
Congenital malformations
Camptodactyly
Ehlers Danlos Syndrome
Contortion
Contortionists
Ehlers Danlos Syndrome
Frontbend
Hypermobility
Joint dislocation
Whiplash (medicine)
Chromosomes
Chromosome 11
X chromosome
Ring chromosome
Chromosome 18
Genodermatoses
(158)
Epidermolysis bullosa
Epidermolytic hyperkeratosis
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
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
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Congenital ichthyosiform erythroderma
Conradi–Hünermann syndrome
Costello syndrome
Craniofacial dysostosis
Cronkhite-Canada 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 dystrophica
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
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
Hailey-Hailey disease
Hallermann-Streiff syndrome
Harlequin type ichthyosis
Hay-Wells syndrome
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
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
Naegeli syndrome
Netherton syndrome
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
Neutral lipid storage disease
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
Peeling skin 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
Sjögren–Larsson syndrome
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 ichthyosis
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
more...
See also
(20)
Nevus flammeus nuchae
Integument
Subcutaneous tissue
Cutis (anatomy)
Autosomal dominant
Autosomal dominant
Autosomal recessive
X linked
DNA repair-deficiency disorder
Corneal dystrophy
Elastin
Cadherin
FBLN5
Connective tissue
Bullous
Tropoelastin
Genetic disorder
ATP7A
Scleroprotein
Elastic fibers
Lysyl hydroxylase
more...
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