Leber Congenital Amaurosis [Leberova kongenitální amauróza]
topical
6
- Terms
-
Leberova kongenitální slepota
-
Amaurosis, Leber Congenital
Congenital Amaurosis of Retinal Origin
Congenital Retinal Blindness
Dysgenesis Neuroepithelialis Retinae
Hereditary Epithelial Dysplasia of Retina
Hereditary Retinal Aplasia
Heredoretinopathia Congenitalis
Leber Abiotrophy
Leber Congenital Tapetoretinal Degeneration
Leber's Amaurosis
Persistent link
https://www.medvik.cz/link/D057130
Definition
A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells.
- DUI
- D057130 MeSH Browser
- CUI
- M0534720
- Previous indexing
- Retinal Diseases (1963-2009)
- History note
- 2010
- Public note
- 2010
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 0
- CO
- complications 0
- DI
- diagnosis 0
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 0
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 0
- GE
- genetics 5
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 0
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 1
- PP
- physiopathology 0
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 5
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records
C
Diseases
C11.270.019
Aicardi Syndrome
C11.270.151
Cone Dystrophy
C11.270.152
Cone-Rod Dystrophies
C11.270.238
Familial Exudative Vitreoretinopathies
C11.768.216
Cone Dystrophy
C11.768.337
Familial Exudative Vitreoretinopathies
C11.768.863
Foveomacular Retinitis