Median cleft face syndrome in association with hydrocephalus, agenesis of the corpus callosum, holoprosencephaly and choanal atresia

1987 ◽  
Vol 146 (3) ◽  
pp. 301-302 ◽  
Author(s):  
T. B�melburg ◽  
W. Lenz ◽  
T. Eusterbrock
1998 ◽  
Vol 28 (5) ◽  
pp. 290-292 ◽  
Author(s):  
Michèle Hamon-Kérautret ◽  
Gustavo Soto Ares ◽  
Xavier Demondion ◽  
Véronique Rouland ◽  
Jean-Paul Francke ◽  
...  

Radiology ◽  
1967 ◽  
Vol 88 (3) ◽  
pp. 473-478 ◽  
Author(s):  
Gerald J. Kurlander ◽  
William DeMyer ◽  
John A. Campbell

1980 ◽  
Vol 64 (2) ◽  
pp. 121-123 ◽  
Author(s):  
V Feiler-Ofry ◽  
V Godel ◽  
P Nemet ◽  
M Lazar

1991 ◽  
Vol 29 (4) ◽  
pp. 279-281 ◽  
Author(s):  
S. Chapman ◽  
P. Weale ◽  
J.H. Goldin ◽  
R.G. Hendel ◽  
A.D. Hockley ◽  
...  

1979 ◽  
Vol 51 (3) ◽  
pp. 397-401 ◽  
Author(s):  
Katsuaki Sakoda ◽  
Susumu Ishikawa ◽  
Tohru Uozumi ◽  
Katsuhiro Hirakawa ◽  
Hideo Okazaki ◽  
...  

✓ A case of sphenoethmoidal meningoencephalocele associated with agenesis of the corpus callosum and median cleft lip and palate in a baby boy is reported. Two other cases have been reported previously presenting exactly the same findings. It is possible that these malformations constitute a distinct type of congenital anomaly.


2012 ◽  
Vol 03 (01) ◽  
pp. 65-67 ◽  
Author(s):  
Seema Sharma ◽  
Vipin Sharma ◽  
Meenakshi Bothra

ABSTRACTThis is a report of a rare case of frontonasal dysplasia (FND) in a full-term girl with birth weight of 2.750 kg. The baby had the classical features of FND. There were no other associated anomalies. There was no history of consanguinity and no family history of similar conditions. So inheritance of this case could be considered sporadic. Maxillofacial surgery should be considered for all patients for whom improvement is possible. However, in developing countries where there are considerable limitations in provision of social services, with economic and educational constraints, correction of such major defects remains a challenging task.


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