scholarly journals Huntington's Chorea: General Practitioners' Knowledge about Individuals' At-risk Status

1989 ◽  
Vol 7 (1) ◽  
pp. 49-52 ◽  
Author(s):  
Sven Asger Sørensen ◽  
Kirsten Fenger
Author(s):  
Donald R. McLean ◽  
Taichi Nihei

SUMMARY:Dopamine (DA) uptake by platelets from 41 patients at risk to develop Huntington’s chorea was assayed and compared to controls. The DA uptake was significantly higher in the at risk group. However, the at risk group did not separate into two distinct subgroups. which reduces the usefulness of the assay as a disease prognosticator.


2000 ◽  
Vol 17 (2) ◽  
pp. 58-69 ◽  
Author(s):  
Sue Fischmann ◽  
John L. Cotterell

AbstractThis study compared perceptions of the school environment, coping and enacted support between Year 10 students identified as educationally at risk (n = 31) and a comparison group of students in the same year level (n = 97), at two periods in the school term. At-risk students perceived the school environment to show significantly less concern for students and used problem-focused coping less frequently than did comparison students. Regardless of risk status, girls used social support more frequently than boys did. At-risk girls accessed peer support more than family support ond also frequently contacted school counsellors to discuss problems. At-risk boys rarely sought support from anyone. Implications for school support programs are twofold. Teachers may need additional professional training in how to employ socially supportive practices. In addition, school counsellors may need to foster informal opportunities for social participation, in order to connect vulnerable boys to peers and adults.


1966 ◽  
Vol 112 (488) ◽  
pp. 723-726 ◽  
Author(s):  
Valerie Cowie ◽  
D. B. Gammack

Huntington's chorea is transmitted by a rare autosomal Mendelian dominant gene. Its hereditary transmission is facilitated by a late onset of the condition in many cases. Often the first signs are not seen until late in the reproductive period, so that it is not uncommon for a patient already to have produced a number of children before the diagnosis is made. On a theoretical basis, 50 per cent. of these offspring are at risk for carrying the gene and consequently for developing the condition themselves.


2016 ◽  
Vol 34 (3) ◽  
pp. 286-294 ◽  
Author(s):  
Cédric Rat ◽  
Gaelle Quereux ◽  
Charlotte Grimault ◽  
Jérémy Fernandez ◽  
Mickael Poiraud ◽  
...  

The Lancet ◽  
1986 ◽  
Vol 327 (8494) ◽  
pp. 1388-1389 ◽  
Author(s):  
L.H. Carrasco ◽  
C.S. Mukherji

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