Cardiovascular Journal of Africa: Vol 21 No 1 (January/February 2010) - page 38

CARDIOVASCULAR JOURNAL OF AFRICA • Vol 21, No 1, January/February 2010
36
AFRICA
P, Gerdes M,
et al
. The Philadelphia story: the 22q11.2 deletion: report
on 250 patients.
Genet Couns
1999;
10
(1): 11–24.
Kyburz A, Bauersfeld U, Schinzel A, Riegel M, Hug M, Tomaske M,
10.
et al
. The fate of children with microdeletion 22q11.2 syndrome and
congenital heart defect: clinical course and cardiac outcome.
Pediatr
Cardiol
2008;
29
(1): 76–83.
Farkas LG.
11.
Anthropometry of the Head and Face
, 2nd edn. New York:
Raven Press, 1994.
Momma K, Kondo C, Matsuoka R. Tetralogy of Fallot with pulmonary
12.
atresia associated with chromosome 22q11 deletion.
J Am Coll Cardiol
1996;
27
(1): 198–202.
Momma K, Kondo C, Matsuoka R, Takao A. Cardiac anomalies associ-
13.
ated with a chromosome 22q11 deletion in patients with conotruncal
anomaly face syndrome.
Am J Cardiol
1996;
78
(5): 591–594.
Hofbeck M, Rauch A, Buheitel G, Leipold G, von der Emde J, Pfeiffer
14.
R,
et al
. Monosomy 22q11 in patients with pulmonary atresia, ventricu-
lar septal defect, and major aortopulmonary collateral arteries.
Heart
1998;
79
(2): 180–185.
Boudjemline Y, Fermont L, Le Bidois J, Lyonnet S, Sidi D, Bonnet D.
15.
Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects:
a 6-year prospective study.
J Pediatr
2001;
138
(4): 520–524.
Lewin MB, Lindsay EA, Baldini A. 22q11 deletions and cardiac disease.
16.
Prog Ped Cardiol
1996;
6
(1): 19–28.
Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon
17.
AP,
et al
. Importance of microdeletions of chromosomal region 22q11
as a cause of selected malformations of the ventricular outflow tracts
and aortic arch: a three-year prospective study.
J Pediatr
1996;
129
(1):
26–32.
Michielon G, Marino B, Formigari R, Gargiulo G, Picchio F, Digilio
18.
MC,
et al
. Genetic syndromes and outcome after surgical correction of
tetralogy of Fallot.
Ann Thorac Surg
2006;
81
(3): 968–975.
Anaclerio S, Di Ciommo V, Michielon G, Digilio MC, Formigari
19.
R, Picchio FM,
et al
. Conotruncal heart defects: impact of genetic
syndromes on immediate operative mortality.
Ital Heart J
2004;
5
(8):
624–628.
Carotti A, Digilio MC, Piacentini G, Saffiro C, Di Donato RM, Marino
20.
B. Cardiac defects and results of cardiac surgery in 22q11.2 deletion
syndrome.
Dev Disabil Res Rev
2008;
14
(1); 35–42.
Ziolkowska L, Kawalec W, Turska-Kmiec A, Krajewska-Walasek M,
21.
Brzezinska-Rajszys G, Daszkowska J,
et al
. Chromosome 22q11.2
microdeletion in children with conotruncal heart defects: frequency,
associated cardiovascular anomalies, and outcome following surgery.
Eur J Pediatr
2008;
167
(10): 1135–1140.
Hastreiter AR, D’Cruz IA, Cantez T, Namin EP, Licata R. I. Right-sided
22.
aorta. Occurrence of right aortic arch in various types of congenital heart
disease. II. Right aortic arch, right descending aorta, and associated
anomalies.
Heart
1966;
28
(6): 722–739.
Czekajska-Chehab E, Uhlig S, Sta
23.
ś
kiewicz G, Mazur-St
ąż
ka E, Torres
A, Gaw
ę
da K,
et al
. Arteria lusoria in patients with a normal and a right-
sided aortic arch diagnosed with multi-slice computed tomography: a
report of two cases.
Folia Morphol
2007;
66
(1): 74–77.
Hiéronimus S, Bec-Roche M, Pedeutour F, Lambert JC, Wagner-Malher
24.
K, Mas JC,
et al
. The spectrum of parathyroid gland dysfunction asso-
ciated with the microdeletion 22q11.
Eur J Endocrinol
2006;
155
(1):
47–52.
Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R,
25.
et al
.
Conotruncal anomaly face syndrome is associated with a deletion within
chromosome 22q11.
J Med Genet
1993;
30
(10): 822–824.
Guyot L, Dubuc M, Pujol J, Dutour O, Philip N. Craniofacial anthropo-
26.
metric analysis in patients with 22q11 microdeletion.
Am J Med Genet
2001;
100
(1): 1–8.
Shprintzen RJ. Velo-cardio-facial syndrome: 30 Years of study.
27.
Dev
Disabil Res Rev
2008;
14
(1): 3–10.
Óskarsdóttir S, Holmberg E, Fasth A, Strömland K. Facial features in
28.
children with the 22q11 deletion syndrome.
Acta Pediatr
2008;
97
(8):
1113–1117.
Digilio MC, Pacifico C, Tieri L, Marino B, Gianotti A, Dallapiccola B.
29.
Audiological findings in patients with microdeletion 22q11 (di George/
velocardiofacial syndrome.
Br J Audiol
1999;
33
(5): 329–333.
Golding-Kushner KJ, Weller G, Shprintzen RJ. Velo-cardio-facial
30.
syndrome: language and psychological profiles.
J Craniofac Genet Dev
Biol
1985;
5
(3): 259–266.
Shprintzen RJ, Goldberg R, Golding-Kushner KJ, Marion RW. Late-
31.
onset psychosis in the velo-cardio-facial syndrome.
Am J Med Genet
1992;
42
(1): 141–142.
Parissis D, Milonas I. Chromosome 22q11.2 deletion syndrome: an
32.
underestimated cause of neuropsychiatric impairment in adolescence.
J
Neurol
2005;
252
(8): 989–990.
1...,28,29,30,31,32,33,34,35,36,37 39,40,41,42,43,44,45,46,47,48,...68
Powered by FlippingBook