- dystrophic dysplasia
- дистрофическая дисплазия
Англо-русский медицинский словарь. 2012.
dystrophic dysplasia
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Dominant dystrophic epidermolysis bullosa — Classification and external resources DiseasesDB 33249 Dominant dystrophic epidermolysis bullosa (also known as Cockayne Touraine disease ) is a skin condition characterized by vesicles and bullae on the extensor surfaces of the extremities … Wikipedia
Multiple epiphyseal dysplasia — Classification and external resources ICD 9 756.56 OMIM 132400 226900 … Wikipedia
Otospondylomegaepiphyseal dysplasia — Classification and external resources OMIM 215150 DiseasesDB 32024 Otospondylomegaepiphyseal dysplasia (OSMED) is an autosomal recessive … Wikipedia
Kniest dysplasia — Classification and external resources ICD 10 Q77.8 OMIM 156550 DiseasesDB … Wikipedia
Clouston's hidrotic ectodermal dysplasia — Classification and external resources OMIM 129500 Clouston s hidrotic ectodermal dysplasia (also known as Alopecia congenita with keratosis palmoplantaris, Clouston syndrome, [1] … Wikipedia
hidrotic ectodermal dysplasia — an autosomal dominant disorder caused by mutations in the GJB6 gene (locus: 13q12), which encodes connexin 30. It is characterized by hypotrichosis; dystrophic, hypoplastic, or absent nails; hyperpigmentation of the skin over joints;… … Medical dictionary
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
3-я хромосома человека — Идиограмма 3 й хромосомы человека 3 я хромосома человека одна из 23 человеческих хромосом, одна из 22 аутосом человека. Хромосома содержит почти 200 млн пар оснований … Википедия
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
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
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
