Diagnosis and treatment of a child with the syndrome of apparent mineralocorticoid excess type 1

1996 ◽  
Vol 85 (1) ◽  
pp. 111-113 ◽  
Author(s):  
J Miiller-Berghaus ◽  
J Homoki ◽  
DV Michalk ◽  
U Querfeld
Diabetes ◽  
2008 ◽  
Vol 57 (5) ◽  
pp. 1312-1320 ◽  
Author(s):  
E. Martinuzzi ◽  
G. Novelli ◽  
M. Scotto ◽  
P. Blancou ◽  
J.-M. Bach ◽  
...  

2021 ◽  
Vol 11 (20) ◽  
pp. 9436
Author(s):  
Abegail Tshivhase ◽  
Tandi Matsha ◽  
Shanel Raghubeer

Maturity-Onset Diabetes of the Young (MODY) is the most common form of monogenic diabetes resulting from a single gene mutation. It is characterized by mild hyperglycemia, autosomal dominant inheritance, early onset of diabetes (<25 years), insulin resistance, and preservation of endogenous insulin secretion. Currently, 14 MODY subtypes have been identified, with differences in incidence, clinical features, diabetes severity and related complications, and treatment response. This type of diabetes is mostly misdiagnosed as either type 1 or type 2 diabetes mellitus because it is difficult to differentiate between these forms of diabetes due to clinical similarities, the high cost of genetic testing, and lack of awareness. As a result, thousands of patients are not receiving appropriate treatment. Accurate diagnosis would allow for more effective therapeutic management and treatment strategies that are distinct from those used for type 1 and type 2 diabetes. This review serves to explore MODY subtypes, diagnosis, and treatment, and increase awareness of MODY incidence.


2014 ◽  
pp. 49-62
Author(s):  
D. G. Kurbatov ◽  
S. A. Dubskiy ◽  
A. E. Lepetukhin ◽  
R. V. Rozhivanov ◽  
J. G. Schwartz

1998 ◽  
Vol 37 (8) ◽  
pp. 491-496 ◽  
Author(s):  
Ann U. Pitel ◽  
Linda Monaco ◽  
Gary R. Geffken ◽  
Janet H. Silverstein

2011 ◽  
Vol 5 (2) ◽  
pp. 136-149 ◽  
Author(s):  
Sonke Detlefsen ◽  
J.-Matthias Lohr ◽  
Asbjorn M. Drewes ◽  
Jens B. Frokjaer ◽  
Gunter Kloppel

2013 ◽  
Vol 88 (5) ◽  
pp. 787-792 ◽  
Author(s):  
Jose Augusto da Costa Nery ◽  
Fred Bernardes Filho ◽  
Juliana Quintanilha ◽  
Alice Miranda Machado ◽  
Soraya de Souza Chantre Oliveira ◽  
...  

A type 1 reaction or reversal reaction is expressed clinically by inflammatory exacerbation of the skin lesions and nerve trunks, consequently leading to sensory and motor alterations. It occurs in non-polar forms of leprosy, although it can occur in a small percentage of sub-polar LL treated patients. Disabilities, deformities and morbidity, still present in leprosy, are mainly caused by these acute episodes. The recognition of reactional states is imperative for an early approach and efficient management, to avoid the emergence of disabilities that stigmatize the disease. This review aims to describe the clinical aspects, immunopathogenesis, epidemiology, histopathological features and therapeutics of type 1 reactions.


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