Asymmetric crying facies and associated congenital anomalies: The contribution of 22q11 microdeletions

Journal of Child Neurology

Volumn 16, Issue 10, 2001, Pages 778-

  Innes, A M ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; CARDIOVASCULAR MALFORMATION; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL MALFORMATION; CONTROLLED STUDY; DIGEORGE SYNDROME; EARLY DIAGNOSIS; ECHOCARDIOGRAPHY; ECHOENCEPHALOGRAPHY; FACE MALFORMATION; FACIES; FLUORESCENCE IN SITU HYBRIDIZATION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; KARYOTYPE; LETTER; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SPINE RADIOGRAPHY; SYNDROME VATER; TERATOLOGY; THORAX RADIOGRAPHY; VELOCARDIOFACIAL SYNDROME;

EID: 0035217564     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380101601016     Document Type: Letter

References (8)

1. Asymmetric crying facies and associated congenital anomalies: Prospective study and review of the literature
2. Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivity
3. Chromosome 22q11 deletion syndrome: An update and review for the primary pediatrician
4. Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletions, including a familial case
5. Cayler cardiofacial syndrome and del 22q11: Part of CATCH 22 phenotype
6. Monozygotic twins concordant for Cayler syndrome
7. Two patients with asymmetric crying facies, normal cardiovascular systems and deletion of chromosome 22q11
8. Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome