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Cet abstract a été assigné à session SBO-BOG Free papers: Genetica/Génétique
TitreMaternally inherited diabetes and deafness associated with ptosis
ButTo report ptosis as an associated finding in two patients with maternally inherited diabetes and deafness (MIDD).
MéthodesTwo female patients with MIDD are described. Both carry the mitochondrial (mt) point mutation A3243G tRNALeu. A detailed ophthalmological examination was performed, including Levator muscle function, vertical fissure height and upper lid crease position measurements, and extensive imaging and functional evaluation.
RésultatsTwo patients, respectively 41 and 47 years old, were referred to us. The first patient complained of a slowly progressive unilateral ptosis. Vertical fissure height was 5 mm for the right eye (RE) and 8 mm for the left eye (LE). Levator muscle function was normal in 2004 and decreased to 11 mm and 12 mm for the RE and LE respectively, suggestive of a myogenic ptosis. Preoperative fundus examination revealed a macular pattern dystrophy, and a diagnosis of MIDD was made. The ptosis of the RE was corrected using levator resection with reinsertion. Three years later, a bilateral ptosis recurred.
The second MIDD patient was referred for bilateral pigment alterations at the posterior pole. A bilateral ptosis was noted, which was myogenic in origin. Gradually the ptosis increased over a 3-year period.
ConclusionMIDD has pleomorphic manifestations, and ptosis should be added to the list of associated clinical features. Early identification of MIDD is important as it facilitates early detection, prevention and treatment of its associated disorders in both patients and their maternal relatives.
Auteur 1
NomROBBERECHT
InitialesKR
InstitutDept of Ophthalmol, Ghent Univ Hosp
VilleGhent
Auteur 2
NomDECOCK
InitialesCE
InstitutDept of Ophthalmol, Ghent Univ Hosp
VilleGhent
Auteur 3
NomSENECA
InitialesS
InstitutCtr Med Gen, Univ Hosp Brussels
VilleBrussels
Auteur 4
NomDE BLEECKER
InitialesJ
InstitutDept of Neurol, Ghent Univ Hosp
VilleGhent
Auteur 5
NomLEROY
InitialesBP
InstitutDept of Ophthalmol & Ctr Med Genet, Ghent Univ Hosp
VilleGhent
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