Nl-Fr

View abstract

This abstract is assigned to session SBO-BOG Free papers: Genetica/Génétique
TitleMaternally inherited diabetes and deafness associated with ptosis
PurposeTo report ptosis as an associated finding in two patients with maternally inherited diabetes and deafness (MIDD).
MethodsTwo 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.
ResultsTwo 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.
Author 1
Last nameROBBERECHT
InitialsKR
DepartmentDept of Ophthalmol, Ghent Univ Hosp
CityGhent
Author 2
Last nameDECOCK
InitialsCE
DepartmentDept of Ophthalmol, Ghent Univ Hosp
CityGhent
Author 3
Last nameSENECA
InitialsS
DepartmentCtr Med Gen, Univ Hosp Brussels
CityBrussels
Author 4
Last nameDE BLEECKER
InitialsJ
DepartmentDept of Neurol, Ghent Univ Hosp
CityGhent
Author 5
Last nameLEROY
InitialsBP
DepartmentDept of Ophthalmol & Ctr Med Genet, Ghent Univ Hosp
CityGhent
top ^