Atypical manifestation of progressive external ophthalmoplegia;Manifestation atypique d'une ophtalmoplégie progressive externe

Klinische Monatsblatter fur Augenheilkunde

Volumn 208, Issue 5, 1996, Pages 366-367

  Rossier, J ^a,b   Hatt, M ^a  

^a CANTONAL HOSPITAL WINTERTHUR   (Switzerland)

^b Kantonsspital ^*

Author keywords

Mitochondrial DNA; Progressive external ophthalmoplegia

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; BIOPSY; CASE REPORT; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; EXTRAOCULAR MUSCLE; FEMALE; FOLLOW UP; GENETICS; HUMAN; PATHOLOGY; PTOSIS;

ADOLESCENT; ADULT; BIOPSY; BLEPHAROPTOSIS; DNA, MITOCHONDRIAL; FEMALE; FOLLOW-UP STUDIES; HUMANS; OCULOMOTOR MUSCLES; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL;

EID: 0030140903     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1035241     Document Type: Article

References (6)

1. Morris MA. Mitochondrial mutations in neuro-ophthalmological diseases. J Clin Neuroophthalmol 1990; 10 (3):159-166
2. Breningstall G. Approach to diagnosis of oxidative metabolism disorders. Pediatr Neurol 1993; 9:81-90
3. Clarke L. Mitochondrial disorders in Pediatrics. Ped Clin North America 1992; 39 (2):319-334
4. Munnich A et al. Clinical aspects of mitochondrial disorders. J Inher Metal Dis 1992; 15:448-455
5. Wallace D. Mitochondrial diseases: genotype versus phenotype. Trends Genet 1993; 9:128-133
6. Kawashima S, Nishizawa M. Multiple mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO). NipponRinsho 1993; 51 (9):2391-2395