Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome

Genetics in Medicine

Volumn 16, Issue 1, 2014, Pages 40-44

  Cheung, Evelyn Ning Man ^a   George, Susan R ^a,b,c   Andrade, Danielle M ^c,d   Chow, Eva W C ^a,e   Silversides, Candice K ^b,c,f,g   Bassett, Anne S ^a,c,d,e,f  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY HEALTH NETWORK   (Canada)

^d TORONTO WESTERN HOSPITAL   (Canada)

^e UNIVERSITY OF TORONTO   (Canada)

^f TORONTO GENERAL HOSPITAL   (Canada)

^g MOUNT SINAI HOSPITAL   (Canada)

Author keywords

22q11 deletion syndrome; cognitive; endocrine; neonatal; outcome

Indexed keywords

ADULT; AORTA ARCH; ARTICLE; BRAIN MALFORMATION; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 22Q11; CONGENITAL HEART DISEASE; DISEASE SEVERITY; DSM-IV; FALLOT TETRALOGY; FAMILY HISTORY; FEMALE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC SERVICE; HUMAN; HYPOCALCEMIA; INFANTILE SPASM; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; NERVE CELL; NEWBORN SCREENING; PHENOTYPE; PREDICTIVE VALUE; YOUNG ADULT;

DIGEORGE SYNDROME; FEMALE; HUMANS; HYPOCALCEMIA; INFANT, NEWBORN; INTELLECTUAL DISABILITY; LOGISTIC MODELS; MALE; NEONATAL SCREENING; RISK FACTORS; SEIZURES; YOUNG ADULT;

EID: 84893532527     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2013.71     Document Type: Article

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