TORCH syndrome: Difference between revisions
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Revision as of 00:54, 23 August 2016
TORCH syndrome is a cluster of symptoms caused by congenital infection with toxoplasmosis, rubella, cytomegalovirus, herpes simplex, and other organisms including syphilis, parvovirus, and Varicella zoster.[1]
Signs and symptoms
Though caused by different infections, the signs and symptoms of TORCH syndrome are consistent. They include hepatosplenomegaly (enlargement of the liver and spleen), fever, lethargy, difficulty feeding, anemia, petechiae, purpurae, jaundice, and chorioretinitis. The specific infection may cause additional symptoms.[1]
TORCH syndrome may develop before birth, causing stillbirth, in the neonatal period, or later in life.[2]
Pathophysiology
TORCH syndrome is caused by in utero infection with one of the TORCH agents, disrupting fetal development.[1]
Treatment
The treatment of TORCH syndrome is mainly supportive and depends on the symptoms present; medication is an option for herpes and cytomegalovirus infections.[1]
Prevention
TORCH syndrome can be prevented by treating an infected pregnant person, thereby preventing the infection from affecting the fetus.[2]
Epidemiology
Developing countries are more severely affected by TORCH syndrome.[2]
References
- ^ a b c d "TORCH Syndrome - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). Retrieved 2016-04-21.
- ^ a b c Neu, Natalie; Duchon, Jennifer; Zachariah, Philip (2015-03-01). "TORCH infections". Clinics in Perinatology. 42 (1): 77–103, viii. doi:10.1016/j.clp.2014.11.001. ISSN 1557-9840. PMID 25677998.