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Pathology Mendelian Disorders: Single-Gene Defects 52a57bad

Phenylketonuria is -

A
AD
B
AR
C
X linked dominant
D
X linked recessive
High-Yield Explanation
Ans. is 'b' i.e., ARAutosomal recessive disordersMetabolicHematologicalEndocrineSkeletalNarvouso Cystic fibrosiso Phenylketonuriao Galactosemiao Homocystinuriao Lysosomal storage diso a1-antitrypsin deficiencyo Wilson diseaseo Hemochromatosiso Glycogen storage disorderso Sickle cell anemiao Thalassemiaso Congenital adrenal hyperplasiao Albinismo EDS (some variants)o Alkaptonuriao Friedreich ataxiao Spinal muscular atrophyo Neurogenic muscular atrophies

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