View abstract

Cet abstract a été assigné à session AOB Poster session1
TitreOcular non-nephropathic cystinosis due to a novel mutation in the lysosomal cystine transporter gene CTNS
Abstract Nr.1025
ButTo describe a patient with ocular cystinosis, a rare AR metabolic disease characterized by the accumulation of cystine crystals, due to a novel mutation in the CTNS gene.
MéthodesA 43-year old lady presented for routine examination. She underwent an extensive clinical and genetic work-up
RésultatsThe patient was in good health. No ocular complaints. The BCVA was 10/10. Slit-lamp examination revealed small white reflective crystals spread in the anterior third of the corneal stroma in both eyes. Fundus examination showed no depigmentation or pigmentary mottling.

Serum protein analysis to exclude a monoclonal gammopathy as cause of the corneal crystals was normal. Laboratory investigations and 24h urine collection showed a normal kidney function. Cystine concentration measured in leucocytes was 0,9 (nl <0,2 nmol half-cystine/mg protein) leading to a diagnosis of ocular, non-nephropathic, cystinosis. Genetic analysis with compound heterzygosity for the 57kb deletion and a novel c.635C>T mutation (p.Ala212Val) in the CTNS gene confirmed the clinical diagnosis.
ConclusionThe incidental finding of corneal crystals warrants a systemic work-up in search for the underlying cause. Renal involvement is heterogeneous in patients with non infantile cystinosis, even within families. Therefore genetic analysis confirming a clinical diagnosis of isolated ocular cystinosis without renal involvement is mandatory for appropriate counselling and treatment.
Auteur 1
NomACCOU
InitialesG.
InstitutUNiversitair ziekenhuis Gent
VilleGent
Auteur 2
NomDe Craene
InitialesS.
InstitutUZ Gent
VilleGent
Auteur 3
NomVanlerberghe
InitialesV
InstitutPrive-praktijk
VilleBeernem
Auteur 4
NomKestelyn
InitialesPh
InstitutUz Gent
VilleGent
Auteur 5
NomLeroy
InitialesBP
InstitutUz Gent
VilleGent
Auteur 6
NomDe Zaeytijd
InitialesJ
InstitutUz Gent
VilleGent
top ^