Age-dependent clinical problems in a Norwegian national survey of patients with the 22q11.2 deletion syndrome

European Journal of Pediatrics

Volumn 169, Issue 8, 2010, Pages 983-989

  Lima, Kari ^a,b   Følling, Ivar ^a   Eiklid, Kristin L ^b   Natvig, Solveig ^b   Abrahamsen, Tore G ^b,c  

^a AKERSHUS UNIVERSITY HOSPITAL   (Norway)

^b OSLO UNIVERSITY HOSPITAL   (Norway)

^c UNIVERSITY OF OSLO   (Norway)

Author keywords

22q11.2 deletion syndrome; Congenital cardiac anomalies; DiGeorge syndrome; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME 22Q11.2 DELETION SYNDROME; CHROMOSOME DELETION; CLINICAL ASSESSMENT; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; FEEDING DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETIC DISORDER; GENITAL MALFORMATION; HEALTH SURVEY; HUMAN; INFANT; KYPHOSCOLIOSIS; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NORWAY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEMI STRUCTURED INTERVIEW; SOCIAL BEHAVIOR; SPEECH DISORDER; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FLUORESCENCE; GENE DELETION; GENITALIA; HUMANS; IN SITU HYBRIDIZATION; INFANT; INFECTION; KIDNEY; LEARNING DISORDERS; MALE; MEDICAL RECORDS; MIDDLE AGED; NORWAY; PHENOTYPE; YOUNG ADULT;

EID: 77954423933     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-010-1161-3     Document Type: Article

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