A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012

Orphanet Journal of Rare Diseases

Volumn 7, Issue 1, 2012, Pages

  Cui, Yazhou ^a,b   Zhao, Heng ^a,b   Liu, Zhenxing ^a,b   Liu, Chao ^a,b   Luan, Jing ^a,b   Zhou, Xiaoyan ^a,b   Han, Jinxiang ^a,b  

^a SHANDONG PROVINCIAL HOSPITAL AFFILIATED TO SHANDONG FIRST MEDICAL UNIVERSITY   (China)

^b BEIJING HOSPITAL   (China)

Author keywords

Bibliographic study; China; Genetic skeletal diseases; Rare diseases

Indexed keywords

ACHONDROPLASIA; ACROCEPHALOSYNDACTYLY; ALBERS SCHOENBERG DISEASE; ARACHNODACTYLY; BONE DISEASE; BRACHYDACTYLY; CAFFEY DISEASE; CAMURATI ENGELMANN DISEASE; CARTILAGE HAIR HYPOPLASIA; CHONDROCALCINOSIS; CHONDRODYSPLASIA; CHONDRODYSPLASIA PUNCTATA; CINCA SYNDROME; CLEIDOCRANIAL DYSPLASIA; CRANIOFACIAL SYNOSTOSIS; CRANIOFRONTONASAL SYNDROME; CRANIOMETAPHYSEAL DYSPLASIA; CROUZON SYNDROME; CURRARINO TRIAD; DE LANGE SYNDROME; DISEASE CLASSIFICATION; DYSOSTOSIS; ECTRODACTYLY; EEC SYNDROME; EHLERS DANLOS SYNDROME; ELLIS VAN CREVELD SYNDROME; ENCHONDROMATOSIS; ENDOSTEAL HYPEROSTOSIS; EPIPHYSIS HEMIMELIC DYSPLASIA; FAMILIAL EXPANSILE OSTEOLYSIS; FAMILIAL HIP DYSPLASIA; FANCONI ANEMIA; FIBROUS DYSPLASIA; FRONTOMETAPHYSEAL DYSPLASIA; FRONTONASAL DYSPLASIA; FUCOSIDOSIS; FUHRMANN SYNDROME; GALACTOSIALIDOSIS; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; GENETIC SKELETAL DISORDER; GEOGRAPHIC DISTRIBUTION; GM1 GANGLIOSIDOSIS; GREBE DYSPLASIA; GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; HAJDU CHENEY SYNDROME; HALLERMANN STREIFF SYNDROME; HANHART SYNDROME I; HOLT ORAM SYNDROME; HUMAN; HYPERPARATHYROIDISM; HYPERTROPHIC OSTEOARTHROPATHY; HYPOCHONDROPLASIA; HYPOPHOSPHATASIA; HYPOPHOSPHATEMIC RICKETS; IMMUNO OSSEOUS DYSPLASIA; JARCHO LEVIN SYNDROME; JUVENILE OSTEOPOROSIS; KLIPPEL FEIL SYNDROME; KNIEST DYSPLASIA; LARSEN SYNDROME; LIPOMEMBRANEOUS OSTEODYSTROPHY WITH LEUKOENCEPHALOPATHY; MANDIBULOFACIAL DYSOSTOSIS; MANNOSIDOSIS; MARFAN SYNDROME; MARSHALL SYNDROME; MECKEL SYNDROME; MESOMELIC DYSPLASIA; MUCOLIPIDOSIS TYPE 2; MUCOPOLYSACCHARIDOSIS; MULTIPLE CANCER; MULTIPLE SULFATASE DEFICIENCY; MULTIPLE SYNOSTOSES SYNDROME; NAGER ACROFACIAL DYSOSTOSIS; NAIL PATELLA SYNDROME; NEUROFIBROMATOSIS; OCULODENTOOSSEOUS DYSPLASIA; OMODYSPLASIA; OSTEOCHONDRITIS DISSECANS; OSTEOCHONDROMA; OSTEOGENESIS IMPERFECTA; OSTEOSCLEROSIS; PAGET BONE DISEASE; PALLISTER HALL SYNDROME; PARIETAL FORAMINA; POLAND ANOMALY; PREAXIAL POLYDACTYLY; PROGERIA; PROGRESSIVE OSSEOUS HETEROPLASIA; PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA; PSEUDOACHONDROPLASIA; PYCNODYSOSTOSIS; PYLE SYNDROME; RADIOULNAR SYNOSTOSIS; RARE DISEASE; REVIEW; SCHWARTZ JAMPEL SYNDROME; SOTOS SYNDROME; SPONDYLOEPIPHYSEAL DYSPLASIA; SPONDYLOMETAPHYSEAL DYSPLASIA; STICKLER SYNDROME; SYMPHALANGIA; SYSTEMIC HYALINOSIS; THANATOPHORIC DWARFISM; THORAX MALFORMATION; THROMBOCYTOPENIA ABSENT RADIUS; TIBIAL HEMIMELIA; TRICHORHINOPHALANGEAL SYNDROME;

BONE DISEASES; CHINA; GENETIC DISEASES, INBORN; HUMANS; PUBLISHING;

EID: 84865228485     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-7-55     Document Type: Review

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