cytomegalic inclusion disease - ορισμός. Τι είναι το cytomegalic inclusion disease
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Τι (ποιος) είναι cytomegalic inclusion disease - ορισμός

GENUS OF VIRUSES
HHV-5; CMV disease; Cytomegaloviral disease; CMV antenatal infection; Cytomegalovirus infection; Cytomegalovirus infections; Cytomegalic inclusion disease; Cytomegalo; Human Herpesvirus Five; Human Cytomegalovirus; Congenital cytomegalovirus; Cytomegalvirus; CMV mononucleosis; Acute cytomegalovirus infection; CMV infectious mononucleosis; Giant cell inclusion disease; Cytomegalovirus infection of skin; Human cytomegalovirus group; Cytomegaloviral
  • Schematic of a ''Cytomegalovirus''
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Cytomegalic inclusion body disease         
MEDICAL CONDITION
Cytomegalic inclusion body disease (CIBD) also known as cytomegalic inclusion disease (CID) is a series of signs and symptoms caused by cytomegalovirus infection, toxoplasmosis or other rare infections such as herpes or rubella viruses. It can produce massive calcification of the central nervous system, and often the kidneys.
I-cell disease         
HUMAN DISEASE
Mucolipidosis II; Inclusion-cell disease; Inclusion cell disease; Inclusion-Cell Disease; Mucolipidosis Ii; ML II; I cell disease; I Cell disease; I Cell Disease
Inclusion-cell (I-cell) disease, also referred to as mucolipidosis II (ML II), is part of the lysosomal storage disease family and results from a defective phosphotransferase (an enzyme of the Golgi apparatus). This enzyme transfers phosphate to mannose residues on specific proteins.
Microvillous inclusion disease         
HUMAN DISEASE
Microvillus inclusion disease; Microvillous atrophy; Davidson's disease; Familial enteropathy; Congenital microvillous atrophy
Microvillus inclusion disease, previously known as Davidson's disease, congenital microvillus atrophy and, less specifically, microvillus atrophy (note: microvillus is often misspelled as microvillous), is a rare genetic disorder of the small intestine that is inherited in an autosomal recessive pattern.

Βικιπαίδεια

Cytomegalovirus

Cytomegalovirus (CMV) (from cyto- 'cell' via Greek κύτος kútos- 'container' + μέγας mégas 'big, megalo-' + -virus via Latin vīrus 'poison') is a genus of viruses in the order Herpesvirales, in the family Herpesviridae, in the subfamily Betaherpesvirinae. Humans and other primates serve as natural hosts. The 11 species in this genus include human betaherpesvirus 5 (HCMV, human cytomegalovirus, HHV-5), which is the species that infects humans. Diseases associated with HHV-5 include mononucleosis and pneumonia, and congenital CMV in infants can lead to deafness and ambulatory problems.

In the medical literature, most mentions of CMV without further specification refer implicitly to human CMV. Human CMV is the most studied of all cytomegaloviruses.

MX2/MXB was identified as a restriction factor for herpesviruses, which acts at a very early stage of the replication cycle and MX2/MXB restriction of herpesvirus requires GTPase activity.