Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: Two case reports

Journal of Medical Case Reports

Volumn 7, Issue , 2013, Pages

  Xiong, Zhimin ^a   Lu, Yanmei ^a   Xue, Jinjie ^a   Luo, Sanchuan ^a   Xu, Xiaojuan ^a   Zhang, Lusi ^a   Peng, Hao ^a   Li, Wei ^a   Chen, Dengming ^b   Hu, Zhengmao ^a   Xia, Kun ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CONDUCTION DEAFNESS; ECHOCARDIOGRAPHY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC COUNSELING; HEAD CIRCUMFERENCE; HEART LEFT VENTRICLE HYPERTROPHY; HUMAN; KARYOTYPE; MALE; MALOCCLUSION; MANDIBLE HYPOPLASIA; MASTOIDITIS; MAXILLA HYPOPLASIA; NUCLEAR MAGNETIC RESONANCE IMAGING; OSTEOLYSIS; OSTEOPOROSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGERIA; SCHOOL CHILD; SHORT STATURE; SKELETON MALFORMATION;

EID: 84874727244     PISSN: None     EISSN: 17521947     Source Type: Journal    
DOI: 10.1186/1752-1947-7-63     Document Type: Article

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