Medicine:Crome syndrome
From HandWiki
| Crome syndrome | |
|---|---|
| Other names | Cataract-nephropathy-encephalopathy syndrome[1] |
| Specialty | Neurology |
Crome syndrome is a rare disease defined by various symptoms, including epilepsy, intellectual disability, eye and kidney problems. It usually causes death in 4 to 8 months.[2]
History
In 1963, a doctor studied two female infants who showed symptoms of intellectual disability, congenital cataracts, epileptic seizures and small stature. The two girls died at the age of 4 and 8 months. The autopsy revealed renal tubular necrosis and encephalopathy.[3]
References
- ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Cataract nephropathy encephalopathy syndrome" (in en). https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1380. Retrieved 29 June 2019.
- ↑ "Crome syndrome". WrongDiagnostics.com. http://www.wrongdiagnosis.com/c/crome_syndrome/intro.htm. Retrieved 2009-04-02.
- ↑ "Crome syndrome". Johns Hopkins University. https://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=218900. Retrieved 2009-04-02.
External links
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