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AD Optic Atrophy - Son 12 year old man. His vision was not correctable to 20/20. There was concern about macular disease.  His was diagnosed with Streff syndrome in NY.   VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM His father and two of his fathers siblings have similar vision loss.
Autosomal Dominant Optic Atrophy - Sonvaatamisi: 46512 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 39612 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 40712 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 43112 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)
Autosomal Dominant Optic Atrophy - Sonvaatamisi: 37012 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 42712 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 48112 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)	Autosomal Dominant Optic Atrophy - Sonvaatamisi: 41112 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)
Autosomal Dominant Optic Atrophy - Sonvaatamisi: 39512 year old man. His vision was not correctable to 20/20. There was concern about possible macula problem.  His was diagnosed with Streff syndrome in NY. VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM The diagnostic criteria for Streff syndrome are not well established, and the validity of this condition has not been recognized by The American Academy of Ophthalmology, The American Academy of Pediatric Ophthalmology, The American Academy of Optometry or The American academy of Pediatrics. (0 hinnangut)
9 faili 1 lehel

12 year old man. His vision was not correctable to 20/20. There was concern about macular disease.  His was diagnosed with Streff syndrome in NY.   VA OD: Dcc20/63 PH20/50-2 NccJ2 VA OS: Dcc20/63 PH20/50-2 NccJ3 IOP: TP: OD:10 OS:15 Time:02:24 PM His father and two of his fathers siblings have similar vision loss.