Juvenile diabetic cheiroarthropathy

1976 ◽  
Vol 13 (1-2) ◽  
pp. 54-67 ◽  
Author(s):  
Andrea Benedetti ◽  
Claudio Noacco
BMJ ◽  
1979 ◽  
Vol 2 (6196) ◽  
pp. 971-972 ◽  
Author(s):  
J R Robertson ◽  
P M Earnshaw ◽  
I W Campbell

1974 ◽  
Vol 84 (4) ◽  
pp. 510-514 ◽  
Author(s):  
Paul Munk ◽  
Melvin H. Freedman ◽  
Henry Levison ◽  
Robert M. Ehrlich

PEDIATRICS ◽  
1974 ◽  
Vol 54 (3) ◽  
pp. 387-387
Author(s):  
George M. Johnson

Forman, Goldstein and Gonel are to be congratulated for their important, succinct paper, "Management of Juvenile Diabetes Mellitus: Usefulness of 24-Hour Fractional Quantitative Urine Glucose" (Pediatrics, 53:257, 1974). For the past five years, on the recommendation of Dr. Donnell B. Etzwiler, we have followed approximately 60 juvenile diabetics using fractional quantitative 24-hour urine glucose values (obtained three or four times a year). As the authors point out, it is unfortunate and often detrimental to the juvenile diabetic that this simple inexpensive test has not gained wide clinical acceptance or even consideration by the physician caring for the juvenile diabetic.


1975 ◽  
Vol 64 (5) ◽  
pp. 773-776
Author(s):  
C. DACOU-VOUTETAKIS ◽  
TH. THOMAIDIS ◽  
E. ROMA ◽  
A. KALPINI-MAVROU ◽  
C. ECONOMOU-MAVROU

2014 ◽  
Vol 125 (5) ◽  
pp. e10
Author(s):  
Margaret Maheandiran ◽  
Shanthini Mylvaganam ◽  
Chiping Wu ◽  
Youssef El-Hayek ◽  
Sonia Sugumar ◽  
...  

Author(s):  
O. V. Nedzvetska ◽  
L. A. Javtushenko ◽  
S. O. Chumak ◽  
O. V. Kuzmina de Gutarra ◽  
S. I. Turchina ◽  
...  

Progression of diabetic retinopathy is associated with a large number of risk factors, and hyperlipidemia is one of the most common. The work is focused on peculiarities of the progression of juvenile diabetic retinopathy (JDR), depending on the presence of concomitant distyroidism in patients with juvenile diabetes mellitus (JDM), the state of lipid metabolism and melatonin production. The aim. To determine the features of the JDR progression depending on the type of concomitant dysthyroidism, the state of lipid metabolism and production of the hormone melatonin. Materials and methods. The examination of three groups of patients was carried out: group 1 (152 patients) included patients in whom JDM proceeded without thyropathy; group 2 (99 patients) included patients with JDM in combination with autoimmune thyroiditis (AIT); group 3 (111 patients) included patients in whom JDM was accompanied by an increased level of thyroid-stimulating hormone (TSH). Results. It was found that the frequency of proliferative diabetic retinopathy (PDR) in the group with JCD and elevated TSH (21.6%) was 2.7 times higher than the frequency of PDR in the group with JDM and AIT (8.1%) and 3.7 times exceeded the frequency of PDD in JDM without distyroidism (5.9%). The greatest violations of all links of lipid metabolism were found in patients with JDM with an increased level of TSH, which contributes to a more pronounced progression of JDR than in patients without thyropathy or concomitant AIT. The average daily excretion of the hormone melatonin (M) among the studied groups was the lowest in patients with PDD with JCD in combination with increased TSH (38.4 ± 2.7 nmol/day) compared with patients with PDD with JCD without thyropathy (48.3 ± 3.8 nmol/day; p <0.01) and with AIT (42.5 ± 5.6 nmol/day; p <0.01), and compared with the control indicator (52.7 ± 5.8 nmol/day; p <0.001). Conclusions. Based on the results obtained it can be concluded that the combination of type 1 JDM with elevated TSH is accompanied by significant disorders of lipid metabolism and melatonin production and this is a risk factor for accelerated progression of JDR. Keywords: juvenile diabetic retinopathy, thyropathy, melatonin production, lipid metabolism.


Joint Disease ◽  
1987 ◽  
pp. 34
Author(s):  
E.C. HUSKISSON ◽  
F. DUDLEY HART

1984 ◽  
Vol 247 (1) ◽  
pp. H132-H138
Author(s):  
S. M. Mueller

Microvascular pathology and sympathetic autonomic dysfunction have been described early in alloxan-induced diabetic juvenile rats. To determine the longitudinal development of these changes and whether insulin treatment can alter them, vascular and sympathetic function were studied in alloxan-induced (42.5 mg/kg) juvenile diabetic rats and saline-treated controls. The rats were examined 1 and 14 days after induction of diabetes. An insulin-treated group was studied with the 14-day group. Hindquarter perfusion with an artificial solution at constant flow/100 g hindquarter wt was used. After 14 days of diabetes mellitus, the diabetic group showed a significantly depressed response to central ischemia (P less than 0.001), maximal vasoconstriction (P less than 0.02), and maximal dilation (P less than 0.001) compared with both the control and insulin-treated group. The threshold response to norepinephrine did not differ. After 1 day of glucose elevation no differences were present between the control and diabetic animals during any of the testing procedures. These results suggest that severe vascular dysfunction develops early in juvenile-onset alloxan diabetes and that it can be prevented with insulin treatment.


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