Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: A prospective study

European Journal of Human Genetics

Volumn 21, Issue 4, 2013, Pages 386-390

  Reinstein, Eyal ^a   Pariani, Mitchel ^a   Bannykh, Serguei ^a   Rimoin, David L ^a   Schievink, Wouter I ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

hereditary disorders of connective tissue; positional headache screening; spontaneous cerebrospinal fluid leak

Indexed keywords

COLLAGEN TYPE 3; COLLAGEN TYPE 3A1; COLLAGEN TYPE 5; COLLAGEN TYPE 5A1; COLLAGEN TYPE 5A2; ESTRONE; FIBRILLIN 1; FOLLICULIN C; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; COHORT ANALYSIS; CONNECTIVE TISSUE DISEASE; CONSULTATION; CONTROLLED STUDY; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; EHLERS DANLOS SYNDROME; FEMALE; GENETIC SCREENING; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JOINT LAXITY; LIQUORRHEA; MALE; MARFAN SYNDROME; MENINGEAL BIOPSY; PREVALENCE; PRIORITY JOURNAL; PROSPECTIVE STUDY; SCHOOL CHILD; SKIN BIOPSY; VISUAL SYSTEM EXAMINATION;

ADOLESCENT; ADULT; AGED; CEREBROSPINAL FLUID RHINORRHEA; CHILD; COLLAGEN TYPE III; COLLAGEN TYPE V; CONNECTIVE TISSUE; CONNECTIVE TISSUE DISEASES; FEMALE; GENETIC DISEASES, INBORN; GENETIC TESTING; HUMANS; MALE; MICROFILAMENT PROTEINS; MIDDLE AGED; PROSPECTIVE STUDIES; PROTO-ONCOGENE PROTEINS; TUMOR SUPPRESSOR PROTEINS;

EID: 84875055752     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.191     Document Type: Article

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