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Home Books - News from other pediatric orthopedics and systemic disease - skeletal dysplasia, connective tissue weight gain disease and other genetically determined diseases and syndromes with orthopedic manifestations of systemic disease - skeletal dysplasia, connective weight gain tissue weight gain disease and other genetically determined diseases and syndromes with orthopedic manifestations of Orthopaedic Edition - News of pediatric orthopedics I Tuesday, 23 March 2010 12:30
Systemic diseases are not always clearly defined. Classifications are in many systemic diseases cancer diagnosis, many classification again as excluding the diagnosis of clear system. Najzaužívanejšiu classification of skeletal dysplasias, the Commission published nomenclature bone diseases at the European Society for Pediatric Radiology, which has undergone many revisions from the original clinical classification mainly on genetic classification. Classification osteochondrodysplasias
Group 1 achondroplasia - tanatoforická dysplasia - achondroplasia - hypochondroplázia 2 spondylodysplastické Severe dysplasia weight gain dysplasia Metatropické 3 - 4 metatropický dwarfizmus dysplasia with short ribs - asfyktizujúca toracická dysplasia (Jeune syndrome) - chondroektodermálna dysplasia (Ellis-van Creveld syndrome-) 5 Group atelosteogenesis - omodysplázií 6 Group 7 Group diastrofických dysplasia dysplasia dyssegmentálnych 8 Kolagenopatie Type II - II and achondrogenéza hypochondrogenéza - spondyloepifýzová dysplasia - Kniestov Syndrome - Stickler syndrome weight gain type 9 Kolagenopatie XI - otospondylomegaepifýzová weight gain dysplasia 10 Other spondyloepi-(meta) - fýzové dysplasia Multiple epiphyseal dysplasia 11 - multiplex epiphyseal dysplasia - pseudoachondroplázia 12 calcificans chondrodysplasia punctata - calcificans chondrodysplasia punctata - rhizomelic type - Zellweger syndrome weight gain - calcificans chondrodysplasia punctata - Conradi-13 Hünermann type metaphyseal dysplasia dysplasia Spondylometafýzová 14 15 16 Brachyolmia spondylodysplázie . Mezomelické weight gain 17 Akromelické dysplasia dysplasia - trichorinofalangový syndrome - brachydaktýlia 18 19 Akromezomelické dysplasia weight gain dysplasia with predominant involvement of flat bones - 20 kleidokraniálna dysplasia dysplasia with bent (kinked) Bone - Dysplasia kamptomelická - Stüve 21-Wiedemann dysplasia dysplasia with multiple dislocations - Larsen syndrome multiple dysostóz Group 22 - 23 mucopolysaccharidosis dysplasia with a reduction in bone density - juvenile osteoporosis - osteogenesis imperfecta weight gain 24 dysplasia with mineralization defects - osteomalacia - renal osteodystrophy - hyper / hypoparathyroidism / pseuodohypoparatyreoidizmus 25 Increased bone density without modification of the shape - meloreostóza - osteopoikília - osteopetrosis 26 Increased bone density DC metaphyseal disabilities - metaphysis dysplasia (Pyle disease) 27 28 Kraniotubulárna weight gain digital dysplasia neonatal severe osteosclerotic dysplasia 29 Fault development cartilaginous and fibrous weight gain components of the skeleton - dysplasia epiphysealis hemimelica (Trevor syndrome) weight gain - multiple osteochondromas - metachondromatóza - multiplex weight gain enchondromatóza (Ollier syndrome) - Mafucciho syndrome - fibrous dysplasia (monostotická, polyostotická, McCune-Albright) - fibrodysplasia weight gain ossificans progressiva - cherubizmus osteolysis 30 - Familial multicentric wrist and carpus / tarsal osteolysis - Torg syndrome - familial expansive osteolysis - Gorham syndrome 31 patellar dysplasia - nail-patella syndrome - Meier-Gorlin syndrome Dysostózy (localized hereditary skeletal deformity)
A. Dysostózy with predominant involvement of the skull and face - Aperto B. Dysostózy syndrome with predominant weight gain involvement of the axial skeleton - Spondylocostal dysplasia (Jarcho-Levin syndrome) C. Dysostózy with predominant involvement of the limbs - Fanconi weight gain syndrome - Coffin-Siris syndrome - Rubinstein-Taybi syndrome, there other right hereditary diseases, which are not included in this classification. They are part of sub-chapters divided according to the following aspects: Chromosomal abnormalities
- Arthrogryposis - pterygiové syndromes - Goldenharov syndrome (syndrome okuloaurikulovertebrálny) - Moebius weight gain Syndrome - Cornelia-de-Lange syndrome - Pierre-Robin syndrome - Williams-Beuren syndrome - Prader-Willi Syndrome - Rett Syndrome - Dandy-walker syndrome Other syndromes with orthopedic manifestations
- Gaucher disease - Neurofibromatosis - Proteus syndrome - Klippel-Trenaunayov syndrome - Marfan syndrome - homocystinuria - Sotos Syndrome - Ehlers-Danlos syndrome - Silver-Russell syndrome - Holt-Oram syndrome - Poland syndrome - hemophilia (A, B, out Willebrand disease ) - hypothyroidism - Weaver syndrome - Beckwith-Wiedemann syndrome
For each of the diagnosis of hereditary not available epidemiological data. In the U.S., shows the incidence of all skeletal dysplasias 25/100, 000 newborns, with the highest incidence oh
Home Books - News from other pediatric orthopedics and systemic disease - skeletal dysplasia, connective tissue weight gain disease and other genetically determined diseases and syndromes with orthopedic manifestations of systemic disease - skeletal dysplasia, connective weight gain tissue weight gain disease and other genetically determined diseases and syndromes with orthopedic manifestations of Orthopaedic Edition - News of pediatric orthopedics I Tuesday, 23 March 2010 12:30
Systemic diseases are not always clearly defined. Classifications are in many systemic diseases cancer diagnosis, many classification again as excluding the diagnosis of clear system. Najzaužívanejšiu classification of skeletal dysplasias, the Commission published nomenclature bone diseases at the European Society for Pediatric Radiology, which has undergone many revisions from the original clinical classification mainly on genetic classification. Classification osteochondrodysplasias
Group 1 achondroplasia - tanatoforická dysplasia - achondroplasia - hypochondroplázia 2 spondylodysplastické Severe dysplasia weight gain dysplasia Metatropické 3 - 4 metatropický dwarfizmus dysplasia with short ribs - asfyktizujúca toracická dysplasia (Jeune syndrome) - chondroektodermálna dysplasia (Ellis-van Creveld syndrome-) 5 Group atelosteogenesis - omodysplázií 6 Group 7 Group diastrofických dysplasia dysplasia dyssegmentálnych 8 Kolagenopatie Type II - II and achondrogenéza hypochondrogenéza - spondyloepifýzová dysplasia - Kniestov Syndrome - Stickler syndrome weight gain type 9 Kolagenopatie XI - otospondylomegaepifýzová weight gain dysplasia 10 Other spondyloepi-(meta) - fýzové dysplasia Multiple epiphyseal dysplasia 11 - multiplex epiphyseal dysplasia - pseudoachondroplázia 12 calcificans chondrodysplasia punctata - calcificans chondrodysplasia punctata - rhizomelic type - Zellweger syndrome weight gain - calcificans chondrodysplasia punctata - Conradi-13 Hünermann type metaphyseal dysplasia dysplasia Spondylometafýzová 14 15 16 Brachyolmia spondylodysplázie . Mezomelické weight gain 17 Akromelické dysplasia dysplasia - trichorinofalangový syndrome - brachydaktýlia 18 19 Akromezomelické dysplasia weight gain dysplasia with predominant involvement of flat bones - 20 kleidokraniálna dysplasia dysplasia with bent (kinked) Bone - Dysplasia kamptomelická - Stüve 21-Wiedemann dysplasia dysplasia with multiple dislocations - Larsen syndrome multiple dysostóz Group 22 - 23 mucopolysaccharidosis dysplasia with a reduction in bone density - juvenile osteoporosis - osteogenesis imperfecta weight gain 24 dysplasia with mineralization defects - osteomalacia - renal osteodystrophy - hyper / hypoparathyroidism / pseuodohypoparatyreoidizmus 25 Increased bone density without modification of the shape - meloreostóza - osteopoikília - osteopetrosis 26 Increased bone density DC metaphyseal disabilities - metaphysis dysplasia (Pyle disease) 27 28 Kraniotubulárna weight gain digital dysplasia neonatal severe osteosclerotic dysplasia 29 Fault development cartilaginous and fibrous weight gain components of the skeleton - dysplasia epiphysealis hemimelica (Trevor syndrome) weight gain - multiple osteochondromas - metachondromatóza - multiplex weight gain enchondromatóza (Ollier syndrome) - Mafucciho syndrome - fibrous dysplasia (monostotická, polyostotická, McCune-Albright) - fibrodysplasia weight gain ossificans progressiva - cherubizmus osteolysis 30 - Familial multicentric wrist and carpus / tarsal osteolysis - Torg syndrome - familial expansive osteolysis - Gorham syndrome 31 patellar dysplasia - nail-patella syndrome - Meier-Gorlin syndrome Dysostózy (localized hereditary skeletal deformity)
A. Dysostózy with predominant involvement of the skull and face - Aperto B. Dysostózy syndrome with predominant weight gain involvement of the axial skeleton - Spondylocostal dysplasia (Jarcho-Levin syndrome) C. Dysostózy with predominant involvement of the limbs - Fanconi weight gain syndrome - Coffin-Siris syndrome - Rubinstein-Taybi syndrome, there other right hereditary diseases, which are not included in this classification. They are part of sub-chapters divided according to the following aspects: Chromosomal abnormalities
- Arthrogryposis - pterygiové syndromes - Goldenharov syndrome (syndrome okuloaurikulovertebrálny) - Moebius weight gain Syndrome - Cornelia-de-Lange syndrome - Pierre-Robin syndrome - Williams-Beuren syndrome - Prader-Willi Syndrome - Rett Syndrome - Dandy-walker syndrome Other syndromes with orthopedic manifestations
- Gaucher disease - Neurofibromatosis - Proteus syndrome - Klippel-Trenaunayov syndrome - Marfan syndrome - homocystinuria - Sotos Syndrome - Ehlers-Danlos syndrome - Silver-Russell syndrome - Holt-Oram syndrome - Poland syndrome - hemophilia (A, B, out Willebrand disease ) - hypothyroidism - Weaver syndrome - Beckwith-Wiedemann syndrome
For each of the diagnosis of hereditary not available epidemiological data. In the U.S., shows the incidence of all skeletal dysplasias 25/100, 000 newborns, with the highest incidence oh
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