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Ophthalmology General c4331ef1

Which is not an AR disorder

A
Gyrate atrophy
B
Goldmann syndrome
C
Bardet-Biedl syndrome
D
Butterfly macular dystrophy
High-Yield Explanation
D i.e. Butterfly macular dystrophy Inheritance of Fundus Dystrophies Autosomal Recessive (AR) Autosomal Dominant (AD) X-linked & variable Macular - Stargardt disease (juvenile - Juvenile Best disease - Alpo syndrome dystrophies macular dystrophy)Q (vitelliform dystrophy) Q (XL dominant) - Fundus flavimaculatus - Adult vitelliform foveomacular - Bietti crystalline - Benign familial fleck retina dystrophy dystrophy (XL or - Labour congenital amaurosis - Familial drusen AR) - Bassen Karzweig syndrome Q - Sorsby pseudoinflammatory - Congenital - Refsum's disease - Usher's syndrome - Bardet-BiedVLaurence Moon Biedl syndrome Q macular dystrophy - Noh Carolina macualr dystrophy - Butterfly macular dystrophy Q - Dominant cystoid macular oedema stationary night blindness (AD,AR or XL) Choroidal - Gyrate atrophyQ - Central areolar choroidal - Choroideremia (x? dystrophies dystrophy linked recessive) - Diffuse choroidal atrophy - Helicoidal parapapillary chorioretinal degeneration - Pigmented paravenous retinochoroidal atrophy (AD, AR, XL, YL) Vitre retino- - Favre - Goldman syndrome Q - Stickler syndrome (Hereditary - Congenital pathies ahro-opthalmopathy retinoschisis (XL) - Erosive vitreoretinopathy - Familial exudative vitreoretinopathy (Criswick Schepens syndrome) AD>>XL recessive.

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