Two patients with Asymmetric Crying Facies, normal cardiovascular systems and deletion of chromosome 22q11

Clinical Dysmorphology

Volumn 6, Issue 2, 1997, Pages 165-169

  Stewart, H S ^a   Clayton Smith, J ^a  

^a ST MARY S HOSPITAL   (United Kingdom)

Author keywords

22q11 deletion; Asymmetric Crying Facies; cardiofacial syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; FACE DYSMORPHIA; FACE MALFORMATION; FEMALE; HEMIFACIAL SPASM; HUMAN; MALE; PRIORITY JOURNAL;

EID: 0030928916     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199704000-00010     Document Type: Article

References (21)

1. Alexiou D, Manolidis C, Papaevangellou G, Nicolopoulos D, Papadatos C (1976): Frequency of other malformations in congenital hypoplasia of depressor anguli oris muscle syndrome. Arch Dis Child 51: 891-893.
2. Bonar BE, Owens RW (1929): Bilateral congenital facial paralysis: Review of the literature and a classification. Am J Dis Child 38: 1256-1272.
3. Cayler GG (1967): An 'epidemic' of congenital facial paresis and heart disease. Pediatrics 40: 666-668.
4. Cayler GG (1969): Cardiofacial Syndrome: Congenital heart disease and facial weakness, a hitherto unrecognised association. Arch Dis Child 44: 69-75.
5. Chantier C, McEnery G (1971): Cardiofacial syndrome. Proc R Soc Med 64: 20-22.
6. Giannotti A, Mingarelli R (1994): Cayler Cardiofacial syndrome and del 22q11: Part of the CATCH22 phenotype. Am J Med Genet 53: 303-304.
7. Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ (1993): Velo-cardio-facial syndrome: A review of 120 patients. Am J Med Genet 45: 313-319.
8. Hepner WR (1951): Some observations on facial paresis in the newborn infant: etiology and incidence. Pediatrics 8: 494-497.
9. Hoefnagel D, Penry JK (1960): Partial facial paralysis in young children. N Engl J Med 262: 1126-1128.
10. Levin SE, Silverman NH, Milner S (1982): Hypoplasia or absence of the depressor anguli oris muscle and congenital abnormalities, with special reference to the cardiofacial syndrome. SA Med J 81: 227-231.
11. Miller M, Hall JG (1979): Familial asymmetric crying facies: Its occurrence secondary to hypoplasia of the depressor anguli oris muscles. Am J Dis Child 133: 743-746.
12. Nelson KB, Eng GD (1972): Congenital hypoplasia of the depressor anguli oris muscle: Differentiation from congenital facial palsy. J Pediatr 81: 16-20.
13. Papadatos C, Alexiou D, Nicolopoulos D, Mikropoulos H, Hadzigeorgiou E (1974): Congenital hypoplasia of depressor anguli oris muscle: A genetically determined condition? Arch Dis Child 49: 927-931.
14. Pape KE, Pickering D (1972): Asymmetric crying facies: An index of other congenital anomalies. J Pediatr 81: 21-30.
15. Parmelee AH (1931): Moulding due to intra-uterine posture: Facial paralysis probably due to such moulding. Am J Dis Child 42: 1155-1159.
16. Perlman M, Reisner SH (1973): Asymmetric crying facies and congenital anomalies. Arch Dis Child 48: 627-629.
17. Scambler PJ, Kelly D, Lindsay E, Williamson R, Goldberg R, Shprintzen R, Wilson DI, Goodship JA, Cross IE, Burn J (1992): Velo cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. Lancet 339: 1138-1139.
18. Silengo MC, Bell GL, Biagioli M, Guala A, Bianco R, Strandoni P, De Sario PN, Franceschini P (1986): Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivity. Clin Genet 30: 481-484.
19. Singhi S, Singhi P, Lall KB (1980): Congenital asymmetrical crying facies. Clin Pediatr 19: 673-678.
20. Trainer AH, Morrison N, Dunlop A, Wilson N, Tolmie J (1996): Chromosome 22q11 microdeletions in tetralogy of Fallot. Arch Dis Child 74: 62-63.
21. Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ (1992): Deletions within chromosome 22q11 in familial congenital heart disease. Lancet 340: 573-575.