Corneal endothelial dysfunction in Pearson syndrome. [electronic resource]
Producer: 20130821Description: 55-7 p. digitalISSN:- 1744-5094
- Acyl-CoA Dehydrogenase, Long-Chain -- deficiency
- Blepharoptosis -- diagnosis
- Child
- Congenital Bone Marrow Failure Syndromes
- Corneal Edema -- diagnosis
- DNA, Mitochondrial -- genetics
- Endothelium, Corneal -- pathology
- Fatal Outcome
- Humans
- Lipid Metabolism, Inborn Errors -- complications
- Male
- Mitochondrial Diseases -- complications
- Muscular Diseases -- complications
- Ophthalmoplegia -- diagnosis
- Retinitis Pigmentosa -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.