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Pathology Mendelian Disorders: Single-Gene Defects cfa1c702

Duchenne muscular dystrophy is inherited as -

A
X linked
B
Autosomal dominant
C
Autosomal recessive
D
Codominant
High-Yield Explanation
Ans. is 'a' i.e., X linked o The two most common forms of muscular dystrophy are X-linked:- Duchenne muscular dystrophy and- Becker muscular dvstrophv.X-linked Recessive disordersMusculoskeletalo Duchene muscular dystrophyo Chronic gramilomatus diseaseHematologicalo Hemophilia A & Bo G-6-PD deficiencyImmuneo Agammaglobulinemiao Wiskott-Aldrich synd.Metabolico Diabetes insipiduso Lesch Nyhan syndromeNervouso Fragile-X-syndromeo Colour blindnessX-linked dominant disorderso Vitamine D resistant ricketso Familial hypophosphatemia

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