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- этимология
Что (кто) такое dystrophia mesodermalis congenita hyperplastica - определение
MEDICAL TERM
Distrophy; Dystrophia; Dystrophy (disambiguation)
Pachyonychia congenita
RARE GROUP OF AUTOSOMAL DOMINANT SKIN DISORDERS THAT ARE CAUSED BY A MUTATION IN ONE OF FIVE DIFFERENT KERATIN GENES
Pachyonychia; Pachyonychia congenita type I; Pachyonychia congenital type I; Jadassohn-Lewandown-Sky syndrome; Pachyonychia congenita type II; Jackson-Lawler pachyonychia congenita; Jackson-Sertoli syndrome; Jackson-Lawler type pachyonychia congenita; Jadassohn–Lewandowsky syndrome; Jackson–Lawler pachyonychia congenita; Jackson–Sertoli syndrome; Jadassohn-Lewandowsky syndrome; Pachyonychia congenita type III; Schafer-Brunauer syndrome; Jackson-Lawler syndrome; Jadasssohn-Lewandowsky syndrome; Jadassohn Lewandowsky syndrome; Pachyonychia congenita Jackson Lawler type; Pachyonychia congenita Jackson–Lawler type; Pachyonychia congenita Jackson-Lawler type; Pachyonychia congenita type 1; Pachyonychia congenita type 2
Pachyonychia congenita (often abbreviated as "PC") is a rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes. Pachyonychia congenita is often associated with thickened toenails, plantar keratoderma, and plantar pain.
AMCD
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![[[Lee Pearson]], a ten-time [[Paralympic Games]] gold medallist born with arthrogryposis](https://commons.wikimedia.org/wiki/Special:FilePath/Lee Pearson, October 2008.jpg?width=200 "[[Lee Pearson]], a ten-time [[Paralympic Games]] gold medallist born with arthrogryposis")
CONGENITAL JOINT CONTRACTURE IN TWO OR MORE AREAS OF THE BODY
Arthrogryposis multiplex congenita; Arthrogryposis due to muscular dystrophy; Arthrogryposis Multiplex congenita due to muscular dystrophy; Arthrogryposis Multiplex due to muscular dystrophy; Arthrogryposis ectodermal dysplasia other anomalies; Arthrogryposis and ectodermal dysplasia; Arthrogryposis epileptic seizures migrational brain disorder; Arthrogryposis IUGR thoracic dystrophy; Arthrogryposis like disorder; Kuskokwim disease; Arthrogryposis like hand anomaly sensorineural; Arthrogryposis like hand anomaly sensorineural deafness; Arthrogryposis-like hand anomaly and sensorineural deafness; Arthrogryposis like hand anomaly and sensorineural deafness; Arthrogryposis, distal, type 6; Cote Adamopoulos Pantelakis syndrome; Trichooculodermovertebral syndrome; TODV syndrome; Alves syndrome; Van Bervliet syndrome; Arthrogryposis multiplex congenita CNS calcification; Arthrogryposis multiplex congenita distal; AMCD; Arthrogryposis multiplex congenita, distal, x-linked; AMCX1; Gordon Syndrome; Arthrogryposis multiplex congenita neurogenic type; AMCN; Arthrogryposis multiplex congenita pulmonary hypoplasia; Fetal akinesia sequence; Fetal akinesia deformation sequence; Arthrogryposis multiplex congenita-pulmonary hypoplasia; Pena-Shokeir syndrome, type 1; Pena-Shokeir syndrome, type I; Arthrogryposis multiplex congenita whistling face; Illum syndrome; Arthrogryposis multiplex congenita, distal type 1; AMCD1; Arthrogryposis, distal, type 1; Distal arthrogryposis, type 1; DA 1; Arthrogryposis multiplex congenita, distal type 2; Arthrogryposis, distal, type 2B; Arthrogryposis multiplex congenita, distal type 2B; Freeman-Sheldon syndrome variant; Arthrogryposis ophthalmoplegia retinopathy; Oculomelic amyoplasia; Arthrogryposis, distal, type 5; Arthrogryposis, distal, type IIB; Arthrogryposis with oculomotor limitation and electroretinal abnormalities; Arthrogryposis renal dysfunction cholestasis syndrome; Arthrogryposis spinal muscular atrophy; Sheldon Hall syndrome; Index rotation flap; Dorsal carpal wedge osteotomy; Congenital contracture; Cote–Adamopoulos–Pantelakis syndrome; Cote-Adamopoulos-Pantelakis syndrome; Distal arthrogryposis; Arthrogriposis; Sheldon–Hall syndrome; Arthrogryposis multiplex with deafness, inguinal hernias, and early death
Active Matrix Color Display (Reference: AMD, LCD)
AMCD
CONGENITAL JOINT CONTRACTURE IN TWO OR MORE AREAS OF THE BODY
Arthrogryposis multiplex congenita; Arthrogryposis due to muscular dystrophy; Arthrogryposis Multiplex congenita due to muscular dystrophy; Arthrogryposis Multiplex due to muscular dystrophy; Arthrogryposis ectodermal dysplasia other anomalies; Arthrogryposis and ectodermal dysplasia; Arthrogryposis epileptic seizures migrational brain disorder; Arthrogryposis IUGR thoracic dystrophy; Arthrogryposis like disorder; Kuskokwim disease; Arthrogryposis like hand anomaly sensorineural; Arthrogryposis like hand anomaly sensorineural deafness; Arthrogryposis-like hand anomaly and sensorineural deafness; Arthrogryposis like hand anomaly and sensorineural deafness; Arthrogryposis, distal, type 6; Cote Adamopoulos Pantelakis syndrome; Trichooculodermovertebral syndrome; TODV syndrome; Alves syndrome; Van Bervliet syndrome; Arthrogryposis multiplex congenita CNS calcification; Arthrogryposis multiplex congenita distal; AMCD; Arthrogryposis multiplex congenita, distal, x-linked; AMCX1; Gordon Syndrome; Arthrogryposis multiplex congenita neurogenic type; AMCN; Arthrogryposis multiplex congenita pulmonary hypoplasia; Fetal akinesia sequence; Fetal akinesia deformation sequence; Arthrogryposis multiplex congenita-pulmonary hypoplasia; Pena-Shokeir syndrome, type 1; Pena-Shokeir syndrome, type I; Arthrogryposis multiplex congenita whistling face; Illum syndrome; Arthrogryposis multiplex congenita, distal type 1; AMCD1; Arthrogryposis, distal, type 1; Distal arthrogryposis, type 1; DA 1; Arthrogryposis multiplex congenita, distal type 2; Arthrogryposis, distal, type 2B; Arthrogryposis multiplex congenita, distal type 2B; Freeman-Sheldon syndrome variant; Arthrogryposis ophthalmoplegia retinopathy; Oculomelic amyoplasia; Arthrogryposis, distal, type 5; Arthrogryposis, distal, type IIB; Arthrogryposis with oculomotor limitation and electroretinal abnormalities; Arthrogryposis renal dysfunction cholestasis syndrome; Arthrogryposis spinal muscular atrophy; Sheldon Hall syndrome; Index rotation flap; Dorsal carpal wedge osteotomy; Congenital contracture; Cote–Adamopoulos–Pantelakis syndrome; Cote-Adamopoulos-Pantelakis syndrome; Distal arthrogryposis; Arthrogriposis; Sheldon–Hall syndrome; Arthrogryposis multiplex with deafness, inguinal hernias, and early death
Activity Monitoring Completion Detection
Википедия
Dystrophy
Dystrophy is the degeneration of tissue, due to disease or malnutrition, most likely due to heredity.
