Full 2L QBank
Pathology Mendelian Disorders: Single-Gene Defects 94b05b9d

Autosomal dominant is -

A
G6PD deficiency
B
Hirshsprung disease
C
Neurofibromatosis
D
Vitamin D resistant rickets
High-Yield Explanation
Ans. is 'c' i.e., Neurofibromatosis Autosomal dominant disordersNervousUrinaryGITHematologicalSkeletalMetabolico Huntington diseaseo Polycystic kidneyo Familial polyposis colio Heriditarv spherocytosiso Marfan syndromeo Familial hypercholesterolemiao Neurofibro-matosiso Gardner's syndromeo Von-Willibrand diso EDS (some variant)o Acute intermittent porphyriao Turcot's syndromeo Myotonic dystrohvo Lynch syndromeo Osteogenesis imperfecta o Peutz Jagher's syndromeo Tuberous sclerosiso Achondroplasiao Juvenile polyposiso Retinoblastoma

Related Pathology MCQs

Practice 2,00,000+ NEET PG Questions Free

Timed mock tests, mistake queue analytics, audio lectures & zero attempt limits on i❤️Exams.

Start Free Mock Test Now