developmental variants
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2021 ◽  
Vol 23 ◽  
pp. 11-22
Author(s):  
Zbigniew Walczak

The paper presents a feasibility analysis of changes in the manner of development a former sports facility, Edmund Szyc Stadium in Poznań. The terrain and adjacent areas were inventoried, including the assessment of inter-area relationships. Based on the inventory and authors' surveys, three developmental variants were selected for further analysis. Particular attention was paid to the purpose of the area in the local zoning plan (local spatial development plan) and the preferences of its local community. A multi-criteria analysis carried out with three different methods – AHP, MAUT and PROMETHEE II indicated the second variant as optimal. Additionally, the authors performed a sensitivity analysis of the AHP method to determine the weight of adopted criteria. This allowed for observing what impact these changes had on the final result. The sensitivity analysis was performed only for 3 main groups of criteria. The implementation of activities planned in the concept will allow for optimal land development, improvement in functionality as well as improvement in visual and landscape characteristics of the city.


Author(s):  
Meshaal Nadeem ◽  
Hina Arif Tiwari ◽  
Kedar Jambhekar ◽  
Hemendra Shah ◽  
Roopa Ram

AbstractThe spleen is the largest lymphatic organ and is responsible for both hematological and immunological functions. Several common etiologies such as trauma, developmental variants, infectious/inflammatory conditions, and benign and malignant lesions can occur in the spleen. The role of imaging modalities such as ultrasound (US), computed tomography (CT), and magnetic resonance imaging (MRI) in diagnosing these conditions continues to evolve. The main objective of this review article is to illustrate the role of imaging in identifying the common and uncommon pathology of the spleen.


Author(s):  
Michael Cordes ◽  
Stephan Coerper ◽  
Torsten Kuwert ◽  
Christian Schmidkonz

: Embryologic developmental variants of the thyroid and parathyroid glands may cause cervical anomalies that are detectable in ultrasound examinations of the neck. For some of these developmental variants, molecular genetic factors have been identified. Ultrasound, as the first-line imaging procedure, has proven useful in detecting clinically relevant anatomic variants. The aim of this article was to systematically summarize the ultrasound characteristics of developmental variants of the thyroid and parathyroid glands as well as ectopic thymus and neck cysts. Quantitative measures were developed based on our own findings and the respective literature. Developmental anomalies frequently manifest as cysts that can be detected by cervical ultrasound examinations. Median neck cysts are the most common congenital cervical cystic lesions, with a reported prevalence of 7% in the general population. Besides cystic malformations, developmental anomalies may appear as ectopic or dystopic tissue. Ectopic thyroid tissue is observed in the midline of the neck in most patients and has a prevalence of 1/100,000 to 1/300,000. Lingual thyroid accounts for 90% of cases of ectopic thyroid tissue. Zuckerkandl tubercles (ZTs) have been detected in 55% of all thyroid lobes. Prominent ZTs are frequently observed in thyroid lobes affected by autoimmune thyroiditis compared with normal lobes or nodular lobes (P = 0.006). The correct interpretation of the ultrasound characteristics of these variants is essential to establish the clinical diagnosis. In the preoperative assessment, the identification of these cervical anomalies via ultrasound examination is indispensable.


Author(s):  
Francesco Catania ◽  
Rebecca Hagen ◽  
Valerio Vitali

ABSTRACTLong-term environmental exposure under selection-free conditions has no consequences for fitness under the neo-Darwinian paradigm but it may provoke adaptive developmental buffering if environmental pressures foster directional organismal changes. To test this hypothesis, we revisited a Mutation Accumulation (MA) experiment where isogenic lines of the ciliate Paramecium were propagated for >40 sexual cycles (∼4 years) in a nearly selection-free and nutrient-rich environment. We find that these MA lines’ somatic genome is enriched with intervening segments of DNA (IESs), which are normally eliminated during germline-soma differentiation. Across independent replicate MA lines, an excess of these somatic IESs fall into a class of epigenetically controlled sequences, map to the same genomic locations, and preferentially disrupt loci that regulate nutrient metabolism. Although further work is needed to assess the phenotypic consequences of somatic IESs, these findings support a model where environmentally induced developmental variants may restore an adaptive fit between phenotype and environment. In this model, positive selection is surprisingly dispensable for adaptation.


2018 ◽  
Vol 115 (47) ◽  
pp. 11941-11946 ◽  
Author(s):  
Erik Trinkaus

Diverse developmental abnormalities and anomalous features are evident in the PleistoceneHomofossil record, varying from minor but rare dental, vertebral, and carpal variants to exceptional systemic disorders. There are currently 75 documented anomalies or abnormalities from 66 individuals, spanning the Pleistocene but primarily from the Late Pleistocene Middle and Upper Paleolithic with their more complete skeletal remains. The expected probabilities of finding these variants or developmental disorders vary from <5% to <0.0001%, based on either recent human incidences or relevant Pleistocene sample distributions. Given the modest sample sizes available for the skeletal or dental elements in question, especially if the samples are appropriately limited in time and geography, the cumulative multiplicative probability of finding these developmental changes is vanishingly small. These data raise questions regarding social survival abilities, differing mortuary treatments of the biologically unusual, the role of ubiquitous stress among these Pleistocene foragers, and their levels of consanguinity. No single factor sufficiently accounts for the elevated level of these developmental variants or the low probability of finding them in the available paleontological record.


2016 ◽  
Vol 40 (6) ◽  
pp. 1182-1190 ◽  
Author(s):  
Akshay D. Baheti ◽  
Ramesh S. Iyer ◽  
Marguerite T. Parisi ◽  
Mark R. Ferguson ◽  
Edward Weinberger ◽  
...  

2015 ◽  
Vol 5 ◽  
pp. 38 ◽  
Author(s):  
William T O’Brien ◽  
Peter Shen ◽  
Paul Lee

Accurate interpretation of cervical spine imagining can be challenging, especially in children and the elderly. The biomechanics of the developing pediatric spine and age-related degenerative changes predispose these patient populations to injuries centered at the craniocervical junction. In addition, congenital anomalies are common in this region, especially those associated with the axis/dens, due to its complexity in terms of development compared to other vertebral levels. The most common congenital variations of the dens include the os odontoideum and a persistent ossiculum terminale. At times, it is necessary to distinguish normal development, developmental variants, and developmental anomalies from traumatic injuries in the setting of acute traumatic injury. Key imaging features are useful to differentiate between traumatic fractures and normal or variant anatomy acutely; however, the radiologist must first have a basic understanding of the spectrum of normal developmental anatomy and its anatomic variations in order to make an accurate assessment. This review article attempts to provide the basic framework required for accurate interpretation of cervical spine imaging with a focus on the dens, specifically covering the normal development and ossification of the dens, common congenital variants and their various imaging appearances, fracture classifications, imaging appearances, and treatment options.


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