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Pseudoxanthoma Elasticum
Pseudoxanthoma elasticum
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Related in the Kosmos
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Abnormalities of dermal fibrous and elastic tissue
(18)
Cutis laxa
Ehlers Danlos Syndrome
Elastosis perforans serpiginosa
Gerodermia osteodysplastica
Marfan syndrome
Marfan syndrome
Osteogenesis imperfecta
Acrodermatitis chronica atrophicans
Anetoderma
Blepharochalasis
Homocystinuria
Linear focal elastosis
Perforating calcific elastosis
Reactive perforating collagenosis
Stretch marks
Striae distensae
Ullrich disease
Verrucous perforating collagenoma
Wrinkly skin syndrome
more...
Autosomal recessive disorders
(16)
Eem syndrome
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Congenital ichthyosiform erythroderma
Kindler syndrome
Xeroderma pigmentosum
Bloom syndrome
Ablepharon macrostomia syndrome
Shwachman syndrome
Harlequin type ichthyosis
Propionic acidemia
Meckel-Gruber syndrome
Netherton syndrome
Usher syndrome
Gerodermia osteodysplastica
more...
Genetic disorders
(36)
Lelis syndrome
Familial cutaneous papillomatosis
Glutaricaciduria
Popliteal pterygium syndrome
DNA repair-deficiency disorder
DNA repair-deficiency disorder
Dermatopathia pigmentosa reticularis
Pallister-Hall syndrome
Thrombocytopenia absent radius
VATER syndrome
Pachyonychia congenita
Multiple hereditary exostoses
Tuberous sclerosis
Hay-Wells syndrome
Prader Willi syndrome
Noonan syndrome
Nail patella syndrome
Progeria
Ataxia telangiectasia
Laurence Moon syndrome
Peutz-jeghers syndrome
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Kindler syndrome
Marfan syndrome
Osteogenesis imperfecta
Ehlers Danlos Syndrome
Bloom syndrome
Ablepharon macrostomia syndrome
Shwachman syndrome
Propionic acidemia
Meckel-Gruber syndrome
Netherton syndrome
Usher syndrome
more...
Diseases and disorders
(54)
Cutaneous conditions
Craniofrontonasal dysplasia
Polyglucosan body disease adult
Progressive osseous heteroplasia
Floating harbor syndrome
Floating harbor syndrome
Ichthyosis
Pachydermo- periostosis
Acanthosis nigricans
Connective tissue diseases
Nevus
Opitz syndrome
X-linked hypophosphatemic rickets
Connective tissue disease
Pemphigus
Cutaneous T cell lymphoma
Naegeli syndrome
Claudication
Myotonic dystrophy type 2
X-linked ichthyosis
Focal dermal hypoplasia
Hailey hailey disease
Vascular disorders
Pick disease of the brain
Prune belly syndrome
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Glutaricaciduria
Marfan syndrome
Cutis laxa
Xeroderma pigmentosum
Osteogenesis imperfecta
Popliteal pterygium syndrome
Ehlers Danlos Syndrome
Dermatopathia pigmentosa reticularis
Pallister-Hall syndrome
Thrombocytopenia absent radius
VATER syndrome
Bloom syndrome
Ablepharon macrostomia syndrome
Multiple hereditary exostoses
Shwachman syndrome
Tuberous sclerosis
Harlequin type ichthyosis
Hay-Wells syndrome
Prader Willi syndrome
Noonan syndrome
Nail patella syndrome
Progeria
Ataxia telangiectasia
Netherton syndrome
Usher syndrome
more...
Causes of death
Aortic dissection
Diseases and disorders
DNA repair-deficiency disorder
Syndromes
(15)
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Marfan syndrome
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Bloom syndrome
Ablepharon macrostomia syndrome
Naegeli syndrome
Hay-Wells syndrome
Prader Willi syndrome
Noonan syndrome
Peutz-jeghers syndrome
Prune belly syndrome
Netherton syndrome
Usher syndrome
more...
ABC transporters
ABCC6
ABCC1
ATP binding cassette
Multidrug resistance- -associated protein
Congenital disorders
Congenital malformations
Proximal femoral focal deficiency
Genetic disorders
Ehlers Danlos Syndrome
Prune belly syndrome
Medicine
Neovascular
Pierre Robin (surgeon)
Venereology
Diseases and disorders
Genodermatoses
(158)
Epidermolysis bullosa
Junctional epidermolysis bullosa (medicine)
Recessive dystrophic epidermolysis bullosa
18q deletion syndrome
Acrocephal- osyndactylia
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
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
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 dystrophica
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
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 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
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
Papulosquamous hyperkeratotic skin diseases
Integument
Subcutaneous tissue
Proof and Experimental Establishment
Proof and Experimental Establishment
Angioid streaks
Autosomal dominant
Autosomal recessive
Pellegrini-Stieda syndrome
Aortic aneurysm
Elastic fibers
The International League of Dermatological Societies
Connective tissue
Hallervorden-spatz syndrome
Cadherin
The Birth-Mark
Papules
Calcification
Hardening of the arteries
The Aorta
more...
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