All individuals with variants in gene FNBP1L

2 entries on 1 page. Showing entries 1 - 2.
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00050695 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, generalized hypotonia, polyphagia, abnormal facial shape, astigmatism, constipation 1 1 Johan den Dunnen
00427662 8 PubMed: Klevering 2005 - M ? Netherlands - - - - - retinal disease At 17 years: macular pigment alterations, atrophic spots in retinal periphery. Age 40: extensive, central and midperipheral atrophy, attenuated vessels Large, absolute central scotomas of 60deg. Nasal constriction Age 17: numerous hyperfluorescent spots throughout retina. Age 27: central hyperfluorescent area due to confluent spots; electroretinogram: 1980: Cone: severely reduced, rod: normal/reduced; 1986: Cone: non-recordable, rod: reduced; 2003 cone and rod: non-recordable 1 1 LOVD
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