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Pathology Mendelian Disorders: Single-Gene Defects 811346a3

Following is transmitted as autosomal dominant disorder -

A
Albinism
B
Sickle cell anemia
C
Hereditary spherocytosis
D
Glycogen storage disease
High-Yield Explanation
Ans. is 'c' i.e., Hereditary spherocytosis o Hereditary spherocytosis is an autosomal dominant disorder,o Other three disorders (given in question) are autosomal recessive.Autosomal dominant disordersNervousUrinaryGITHematologicalSkeletalMetabolico Huntington diseaseo Polycystic kidneyo Familial polyposis colio Heriditary sph-erocytosiso Marfan synd-romeo Familial hypercho-lesterolemiao Neurofibro-matosis o Gardner's syndromeo Von-Willibrand diso EDS (some variant)o Acute intermittent porphyriao Myotonic dys-trohy o Turcot's syndrome o Osteogenesis imperfecta o Tuberous scle-rosis o Lynch syndrome o Achondroplasia o Retinoblastoma o Peutz Jagher's syndrome o Juvenile polyposis

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