Paciente con enfermedad corneal severa en el contexto del síndrome KID / Patient with severe corneal disease in KID syndrome
Arch. Soc. Esp. Oftalmol
; 81(4): 225-228, abr. 2006. ilus
Article
in Es
| IBECS
| ID: ibc-046750
Responsible library:
ES1.1
Localization: ES1.1 - BNCS
RESUMEN
Caso clínico Mujer de 33 años con neovascularizacióncorneal bilateral superficial y profunda yqueratopatía punteada superficial de distribucióndifusa, queratoeritema y sordera neurosensorial,que es diagnosticada de síndrome KID.Discusión:
El síndrome KID es una displasia congénitaectodérmica caracterizada por la asociaciónde queratitis vascularizante, lesiones cutáneashiperqueratósicas y sordera neurosensorial. Recientemente,la deficiencia de stem cell limbares ha sidoreconocida como posible factor patogenético claveABSTRACT
Case report A 33-year-old woman with superficial ;;and deep bilateral corneal vascularization and ;;keratoconjunctivitis sicca, keratoerythema and neurosensory ;;deafness, was diagnosed with keratitisichthyosis- ;;deafness (KID) syndrome. ;;Discussion:
KID syndrome is a congenital ectodermal ;;dysplasia characterized by the association of ;;vascularizing keratitis, hyperkeratotic skin lesions ;;and sensorineural hearing loss. Recently, limbal ;;stem cell deficiency was recognized as a possible ;;major pathogenetic factor
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Keratitis, Dendritic
/
Corneal Neovascularization
Limits:
Adult
/
Female
/
Humans
Language:
Spanish
Journal:
Arch. Soc. Esp. Oftalmol
Year:
2006
Document type:
Article
Institution/Affiliation country:
Hospital Municipal de Badalona/España
/
Universidad Autónoma de Barcelona/España