The abnormal individual.

2006 ◽  
pp. 809-831
Author(s):  
Shepherd Ivory Franz
Keyword(s):  
Abnormal Individual

Developmental biodynamics

2017 ◽  
Author(s):  
James Watkins
Keyword(s):  
Functional Ability ◽  
Movement Pattern ◽  
Human Movement ◽  
Energy Resources ◽  
Environmental Constraints ◽  
Task Constraints ◽  
Systems Perspective ◽  
System Components ◽  
Abnormal Individual ◽  
The Individual

From a dynamical systems perspective, coordination of human movement emerges from the intrinsic self-organizing properties of the dynamical system consisting of the individual, the task, and the environment. The movement pattern that emerges depends upon the state of the system components which impose constraints on the types of movement that may emerge. These constraints arise from the anthropometry and functional ability of the individual (individual constraints), the requirements of the task (task constraints), and the prevailing environmental conditions (environmental constraints). Abnormal movement due to cerebral palsy, disease, or injury is likely to be due to abnormal individual constraints in the form of abnormal energy resources. Therapy directed at normalizing the abnormal energy resources is likely to be more effective than therapy directed at normalizing the abnormal kinematics.

The Characterisation of Individuals with Respect to Wilson's Disease

1974 ◽  
Vol 23 (S1) ◽  
pp. 315-324
Author(s):  
Sean O'Reilly
Keyword(s):  
Wilson’S Disease ◽  
False Negative ◽  
Wilson's Disease ◽  
Whole Body ◽  
Intestinal Excretion ◽  
Negative Results ◽  
Liver Copper ◽  
False Negative Results ◽  
Prolonged Retention ◽  
Abnormal Individual

In the case of heredo-familial diseases it is desirable to identify the abnormal genotype, the homozygously abnormal individual, if possible while still asymptomatic, and the carrier of the abnormal gene or allele, the heterozygote.So far as Wilson's disease is concerned, it is possible to diagnose individuals as presymptomatic homozygotes by finding Kayser-Fleischer corneal rings on slit-lamp microscopy, or by demonstrating increased liver-copper on needle biopsy.False-negative results are common, however, and more reliable identification of the presymptomatic homozygote as well as the heterozygote can be achieved by studies of the physiology of copper, using tracer doses of radioactive copper, 67copper, which has a physical half life of about 61 hours. Using this method it can be shown:1. That there is prolonged retention of copper in the whole body in both homozygotes and heterozygotes, the former showing more prolonged retention than the latter.2. In both there is retention of copper in the liver, again more marked in the homozygote than in the heterozygote.3. There is decreased intestinal excretion of copper in both cases as manifested by decreased biliary radiocopper and decreased stool radiocopper, and again this is most marked in the homozygote.4. Urinary excretion of radiocopper is usually increased significantly in the homozygote, but is usually normal or only very slightly increased in the heterozygote.5. The additional finding of impaired ceruloplasmin biosynthesis is sufficient usually to distinguish with certainty between the presymptomatic homozygote and the heterozygote.

The type specimen of Murexia longicaudata (Dasyuromorphia : Dasyuridae): an enigma

2020 ◽  
Vol 42 (3) ◽  
pp. 359
Author(s):  
P. A. Woolley
Keyword(s):  
Type Specimen ◽  
Genetic Studies ◽  
Abnormal Individual

Examination of the skull and dentaries of the type specimen of Murexia longicaudata has led to the conclusion that the holotype is either a highly abnormal individual or that the skull and dentaries are mismatched. The dentaries may be those of a smaller individual. The matter might be resolved if genetic studies were to be carried out on both.

scholarly journals The modulatory effect of cell–cell contact on the tumourigenic potential of pre-malignant epithelial cells: a computational exploration

2013 ◽  
Vol 10 (78) ◽  
pp. 20120703 ◽  
Author(s):  
D. C. Walker ◽  
J. Southgate
Keyword(s):  
Epithelial Cells ◽  
Single Cell ◽  
Pathological Process ◽  
Cell Contact ◽  
Metastasis Suppressor ◽  
Genetic Changes ◽  
Computational Exploration ◽  
Regulation Mechanisms ◽  
Abnormal Individual ◽  
E Cadherin

Malignant development cannot be attributed alone to genetic changes in a single cell, but occurs as a result of the complex interplay between the failure of cellular regulation mechanisms and the presence of a permissive microenvironment. Although E-cadherin is classified as a ‘metastasis suppressor’ owing to its role in intercellular adhesion, the observation that it may be downregulated at a premalignant stage is indicative of additional roles in neoplastic development. We have used an agent-based computational model to explore the emergent behaviour resulting from the interaction of single and subpopulations of E-cadherin-compromised cells with unaffected normal epithelial cells within a monolayer environment. We have extended this to investigate the importance of local tissue perturbations in the form of scratch-wounding, or ablation of randomly-dispersed normal cells, on the growth of a single cell exhibiting E-cadherin loss. Our results suggest that the microenvironment with respect to localized cell density and normal/E-cadherin-compromised neighbours is crucial in determining whether an abnormal individual cell proliferates or remains dormant within the monolayer. These predictions raise important questions relating to the propensity for individual mutations to give rise to disease, and future experimental exploration of these will enhance our understanding of a complex, multifactorial pathological process.

scholarly journals Morphological abnormality in a Longnose Stingray Hypanus guttatus (Bloch & Schneider, 1801) (Myliobatiformes: Dasyatidae)

2019 ◽  
Vol 19 (4) ◽  
Author(s):  
Kurt Schmid ◽  
Marcelo Andrade ◽  
Fabiola Machado ◽  
Juliana Araujo ◽  
Eglé Corrêa ◽  
...  
Keyword(s):  
River Mouth ◽  
Amazon River ◽  
Brazilian Coast ◽  
Morphological Abnormality ◽  
Pectoral Fin ◽  
Term Survival ◽  
First Report ◽  
Northern Brazil ◽  
Abnormal Individual

Abstract: A Longnose stingray Hypanus guttatus (Bloch & Schneider, 1801) embryo with a major asymmetrical morphological abnormality to its pectoral fin was obtained from commercial shrimp fisher's bycatch, off the coast of the Amazon River Mouth in northern Brazil. The specimen and the deformity, which would presumably have impeded its long-term survival, are described and documented in detail. We herein provide the first report of an abnormal individual of this species for the Brazilian coast.

scholarly journals UV-reflectivity of parafocal eyespot elements on butterfly wings in normal and abnormal specimens

2004 ◽  
Vol 15 (1) ◽  
Author(s):  
Mouyu Yang ◽  
Ahti Pyörnilä ◽  
V. Benno Meyer-Rochow
Keyword(s):  
Wild Type ◽  
Type Specimens ◽  
Structural Coloration ◽  
Butterfly Wings ◽  
Abnormal Individual ◽  
Wing Scales ◽  
Cross Vein ◽  
Normal Wild Type

An unusual specimen of Aglais urticae, lacking characteristic UV-reflecting parafocal eyespot elements along the margins of both fore and hind wings, is compared with normal, wild-type specimens. Wing scales, responsible for generating structural coloration, aremissing in the abnormal individual and have been replaced with a type that is typical of pigment-based colours. Other modifications seen in the abnormal specimen include firstly, a distal expansion of a uniformly brown region, that otherwise occupies a proximal position on the hind wings of the wild type, and secondly, the lack of a characteristic orange cross-vein band that runs proximal to the parafocal eyespot elements on the hindwing. The differences in coloration between abnormal and wild type are seen as evidence of a proximal-distal developmental axis (originally proposed by Nijhout 1991) and support a view recently aired by Beldade and Brakefield (2003). It is now clear that studies on butterfly eyespot development must consider not only pigmentcontaining scales, but also the structurallymodified scales responsible for physical colours, i.e. UV reflectivity.

Subclinical Neuromuscular Transmission Abnormality Detected by Single-Fibre EMG is More Pronounced in Cluster Headache Than in Migraine With Aura

Cephalalgia ◽  
2007 ◽  
Vol 27 (7) ◽  
pp. 788-792 ◽  
Author(s):  
A Coban ◽  
MB Baslo ◽  
B Baykan ◽  
K Tutkavul ◽  
EK Orhan ◽  
...  
Keyword(s):  
Cluster Headache ◽  
Migraine With Aura ◽  
Neuromuscular Transmission ◽  
Primary Headache ◽  
Single Fibre ◽  
Voluntary Contraction ◽  
Functional Abnormality ◽  
Control Subjects ◽  
Healthy Control ◽  
Abnormal Individual

The aim was to investigate neuromuscular transmission (NMT) by single-fibre EMG (SFEMG) in a large series of patients having migraine with aura (MA) or cluster headache (CH). Recent studies using SFEMG have shown subclinical dysfunction of NMT in MA and CH. Forty-three patients having MA, 51 with CH and 38 healthy control subjects underwent nerve conduction studies, EMG and SFEMG during voluntary contraction of the extensor digitorum communis muscle. Twenty different potential pairs were recorded and individual, mean and total abnormal individual jitter values were calculated. The results obtained from MA patients were compared with those from CH patients. In MA patients, 32 of 860 jitters were abnormally high, whereas 73 of 1020 of the jitters showed this abnormality in CH patients. None of the control subjects, five MA patients (11.6%) and 11 CH patients (21.6%) were designated as having subclinical NMT abnormality. Thus, patients having junction dysfunction were significantly more common in the CH group. The subclinical NMT abnormality shown by SFEMG is more common in CH than in MA. These two primary headache syndromes may have some shared functional abnormality of NMT constituents which is more evident in CH.

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