scholarly journals Sequel of a Case of Sclerodermia of the Extremities (Sclerodactylia, Acroteric Sclerodermia of Hutchinson) Associated with a Previous and Family History of Angioneurotic Œdema

1910 ◽  
Vol 3 (Clin_Sect) ◽  
pp. 33-35
Author(s):  
T. D. Savill
1982 ◽  
Vol 27 (4) ◽  
pp. 309-311 ◽  
Author(s):  
R. P. Brettle ◽  
R. E. Dunmow ◽  
L. A. Milne ◽  
P. L. Yap

A patient presented at the age of 72 years with a life long history of at least 60 years of abdominal crises described by the patient as ‘bilious vomiting or migraine’. However, a careful clinical and family history suggested a diagnosis of hereditary angioneurotic oedema and this was confirmed by complement studies. Treatment with oral ethinyltestosterone (Danazol) was successful in abolishing her attacks, initially at a dose of 600 mg. per day and latterly at the low dose of200 mg per day.


1982 ◽  
Vol 25 (4) ◽  
pp. 482-486 ◽  
Author(s):  
Robin A. Seider ◽  
Keith L. Gladstien ◽  
Kenneth K. Kidd

Time of language onset and frequencies of speech and language problems were examined in stutterers and their nonstuttering siblings. These families were grouped according to six characteristics of the index stutterer: sex, recovery or persistence of stuttering, and positive or negative family history of stuttering. Stutterers and their nonstuttering same-sex siblings were found to be distributed identically in early, average, and late categories of language onset. Comparisons of six subgroups of stutterers and their respective nonstuttering siblings showed no significant differences in the number of their reported articulation problems. Stutterers who were reported to be late talkers did not differ from their nonstuttering siblings in the frequency of their articulation problems, but these two groups had significantly higher frequencies of articulation problems than did stutterers who were early or average talkers and their siblings.


2001 ◽  
Vol 120 (5) ◽  
pp. A442-A442
Author(s):  
P TSIBOURIS ◽  
M HENDRICKSE ◽  
P ISAACS

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