Crome syndrome
| 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 mental retardation, congenital cataracts, epileptic fits 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". www.orpha.net. Retrieved 29 June 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "Crome syndrome". WrongDiagnostics.com. Retrieved 2009-04-02.
- ^ "Crome syndrome". Johns Hopkins University. Retrieved 2009-04-02.
External links
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