hereditary hyperfunction disorders of endocrine cells
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Disease group (etiology)
Articles
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hereditary hyperfunctions of endocrine cells
19 June 2004 -
WT1-associated diseases
11 May 2004WT1 mutations-associated disorders, WT1-related diseases, WT1-related disorders
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arboviroses
6 February 2006Exemples
yeloow fever
dengue
chikungunya
Kyasanur Forest disease
PAthogeny
Etiologic agents of arboviral diseases are primarily zoonotic pathogens that are maintained in nature in cycles involving arthropod transmission among a variety of susceptible reservoir hosts.
In the simplest form of human exposure, spillover occurs from the enzootic cycle when humans enter zoonotic foci and/or enzootic amplification increases circulation near humans.
Examples include Eastern equine (...) -
echinococcosis
5 December 2005hydatid disease
Definition: Echinococcosis, which is often referred to as hydatid disease or echinococcal disease, is a parasitic disease that affects both humans and other mammals, such as sheep, dogs, rodents and horses.
Images
hepatic cystic echinococcosis / Echinococcus granulosus
https://twitter.com/RhondaYantiss/status/851519941299851265
There are three different forms of echinococcosis found in humans, each of which is caused by the larval stages of different species of the (...) -
inborm errors of thyroid metabolism
21 November 2005Types
TSH unresponsiveness
iodine tranposrt defect
organification defect
coupling defect
anomalies of thyroglobulin synthesis and secretion
deiodinase defect
anomalies of thyroid hormone transport
other defects
See also
Thyroid -
defective iodide transport diseases
23 November 2005Synopsis
large congenital goiter (up to 150 g).
hypothyroidism
atypical cells
hyperplastic pattern with predominant microfollicular aspect
Electron microscopy
hyperactive follicular cell with folding of the basal membrane
See also
NIS symporter protein mutations
References
Camargo RY, Gross JL, Silveiro SP, Knobel M, Medeiros-Neto G. Pathological Findings in Dyshormonogenetic Goiter with Defective Iodide Transport. Endocr Pathol. 1998 Autumn;9(3):225-233. PMID: (...) -
thyroid metabolism diseases
23 November 2005inherited disorders of thyroid metabolism, inborn errors of thyroid metabolism
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cerebral vascular diseases
11 November 2004Exemples
cerebral hemorrhage -
hepatic storage diseases
15 June 2004Digital cases
Case 247 : glycogen storage disease type 3 - GSD3
Types
mucopolysaccharidoses
mannosidosis/fucosidosis
sialidosis
mucolipidosis
GM1 general gangliosidosis
cystinosis
metachromatic leukodystrophy
Farber disease
glycogen storage diseases glycogen storage disease type 1 (GSD1) glycogen storage disease type 2 (GSD2) glycogen storage disease type 3 (GSD3) glycogen storage disease type 4 (GSD4)
hepatic lysosomal storage diseases Wolman disease Gaucher (...) -
multiple endocrine neoplasia syndromes
19 May 2004MENs