- transient bullous dermolysis of newborn
- a rare form of dominant epidermolysis bullosa dystrophica that occurs in newborns but clears up around six months of age.
Medical dictionary. 2011.
Medical dictionary. 2011.
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Osteogenesis imperfecta — Classification and external resources The classic blue sclerae of a person with osteogenesis imperfecta ICD 10 Q … Wikipedia
Ehlers–Danlos syndrome — Classification and external resources The collagen fibril and EDS. (a) Normal collagen fibrils are of uniform size and spacing. Fibrils from a patient with dermatosparaxis (b) show dramatic alterations in fibril morphology with severe effects on… … Wikipedia
Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or … Wikipedia
Fuchs' dystrophy — Classification and external resources Fuchs corneal dystrophy. Light microscopic appearance of the cornea showing numerous excrescences (guttae) on the posterior surface of Descemet s membrane and the presence of cysts in the corneal epithelium… … Wikipedia
Otospondylomegaepiphyseal dysplasia — Classification and external resources OMIM 215150 DiseasesDB 32024 Otospondylomegaepiphyseal dysplasia (OSMED) is an autosomal recessive … Wikipedia
Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… … Wikipedia
Dermatopathia pigmentosa reticularis — Classification and external resources OMIM 125595 Dermatopathia pigmentosa reticularis (also known as Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans, Dermatopathia pigmentosa reticularis hypohidotica et atrophica, and… … Wikipedia
Marshall syndrome — Classification and external resources OMIM 154780 DiseasesDB 31965 Marshall syndrome is a genetic disorder of the connec … Wikipedia
Collagenopathy, types II and XI — The type II and XI collagenopathies are a group of disorders that affect connective tissue, the tissue that supports the body s joints and organs. These disorders are caused by defects in type II or type XI collagen. Collagens are complex… … Wikipedia