A rare brain developmental anomaly in a patient with Usher’s syndrome

2008 ◽  
Vol 30 (1) ◽  
pp. 85-88 ◽  
Author(s):  
Helin Deniz Demir ◽  
Fatih Ersay Deniz ◽  
Hüseyin Yardım
2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Parkash Mandhan ◽  
Amer Al Saied ◽  
Mansour J. Ali

Congenital diaphragmatic hernia is a common developmental anomaly encountered by paediatric surgeons. It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we report a newborn born with concurrent congenital diaphragmatic hernia, Meckel’s diverticulum, and heterotopic pancreatic tissue. This is the first case report of such a triad with description of possible mechanisms of the development.


2008 ◽  
Vol 24 (4) ◽  
pp. 273-279 ◽  
Author(s):  
S. Karjalainen ◽  
M. Teräsvtrta ◽  
J. KÄRJÄ ◽  
H. Kääriäinen
Keyword(s):  

Eye ◽  
2001 ◽  
Vol 15 (3) ◽  
pp. 335-336
Author(s):  
Hirokazu Ohashi ◽  
Ryoji Yamakawa

2003 ◽  
Vol 73 (5) ◽  
pp. 356-360 ◽  
Author(s):  
Gavin D. Sandercoe ◽  
Geoff L. Brooke-Cowden

Author(s):  
N. D. Hastie ◽  
K. Pritchard Jones ◽  
W. Bickmore ◽  
D. Porteous ◽  
V. van Heyningen

Author(s):  
Ramakrishnan Narayanaswamy

<p class="abstract"><span lang="EN-US">Lingual Thyroid is a rare developmental anomaly. It is the most common benign mass found at the junction of the anterior two third and the posterior one third of the tongue. It requires to be excised if it becomes symptomatic by becoming a goiter. It is usually treated medically by thyroxin suppression therapy. However, in cases where the response to medical treatment is poor, it can be excised or transposed. We present a case report of a 28-year-old female with Lingual thyroid who underwent a novel surgical cervical transposition procedure with good result.</span></p>


2013 ◽  
Vol 58 (1-2) ◽  
pp. 19-28
Author(s):  
Julita Templin ◽  
Teresa Napiórkowska

Abstract Oligomely is a type of developmental anomaly occurring in embryos of the spider Tegenaria atrica C.L. Koch under the teratogenic influence of temperature. This anomaly is of metameric origin, as it results from a disorder of metamere formation on the germ band during embryogenesis, resulting in the absence of one half or the whole metamere. In such a case, one or more appendages are missing on one or both sides of the body in a spider leaving a chorion. This anomaly induces changes both in the anatomical structure and exoskeleton of a spider (deformation of carapace and sternum). Carapace length and sternum area were measured, as well as the duration of the subsequent nymph stages of oligomelic individuals with one of the walking appendages missing (always on the right side of the body) was recorded. The consecutive nymph stages of oligomelic individuals lasted for a much shorter time compared with control specimens. This acceleration of development is probably to offset losses incurred during embryogenesis. In the early postembryogenesis, oligomelic specimens exhibited shorter carapace length and smaller surface area of the sternum compared to control individuals, which resulted from the lack of half of the metamere corresponding to the missing leg. However, in older nymph stages, a strong tendency for the faster growth of both carapace and sternum was observed, which can be defined as a compensatory growth increase making up for the losses caused by the anomaly.


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