Open and Closed Lip Schizencephaly in Seckel Syndrome: A Case Report

2009 ◽  
Vol 25 (4) ◽  
pp. 494-496 ◽  
Author(s):  
Rajoo Thapa ◽  
Debkrishna Mallick ◽  
Biswajit Biswas ◽  
Apurba Ghosh
Keyword(s):  
Urology ◽  
2018 ◽  
Vol 120 ◽  
pp. 241-243
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Lily Wang ◽  
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...  

2012 ◽  
Vol 34 (3) ◽  
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Mark O’Driscoll ◽  
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2018 ◽  
Vol 7 (3) ◽  
pp. 223
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...  

2009 ◽  
Vol 56 (6) ◽  
pp. 717
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Tae Hee Kim ◽  
Young Uk Kim ◽  
Jun Gol Song ◽  
Jai Hyun Hwang

2016 ◽  
Vol 14 (03) ◽  
pp. 122-125
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Reza Jalli ◽  
Saeedeh Haghbin
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2018 ◽  
Vol 10 (2) ◽  
pp. 39-42
Author(s):  
Chaitanya R Uppin

Seckel syndrome, first defined by Seckel in 1960, is a rare (incidence 1:10,000) genetically heterogeneous autosomal recessive disorder presenting at birth. Seckel described the disease on the basis of two cases he had studied in Chicago as well as 13 cases on nanocephalic dwarfs reported in the literature over a 200-year period. It is Characterized by dwarfism prenatally resulting in low birth weight, abnormally small head with a “bird‑headed” like appearance (beaked nose, receding forehead, prominent eyes, and micrognathia) and mental retardation. Other facial features include abnormally large eyes and narrow face. This syndrome has an autosomal recessive pattern of inheritance. A case of Seckel syndrome that was reported is described in this article.


2004 ◽  
Vol 13 (1) ◽  
pp. 53-55 ◽  
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Z??beyir Kilic ◽  
Ener Cagri Dinleyici ◽  
Ayten Yakut ◽  
Nesrin Dogruel

2005 ◽  
Vol 15 (4) ◽  
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VIJAYLAKSHMI KAMAT ◽  
JYOTSNA MURTHY ◽  
SYED ALTAF HUSSAIN

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