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Unknown General d8519f6f

The only condition associated with X-linked recessive inheritance is:

A
Phenylketonuria
B
Mucopolysaccharidosis
C
Achondroplasia
D
Marfan's syndrome
High-Yield Explanation
X-linked recessive inheritance Hemophilia-A   Muscular dystrophy   Mucopolysaccharidosis type II (Hunter syndrome) Colour blindness   G6PD deficiency.   X-linked dominant inheritance Hypophosphatemic rickets Incontinentia pigmenti.   Autosomal recessive inheritance   Sickle cell anaemia 0-thalassemia Wilson's disease    Xeroderma pigmentosa   Inborn error of metabolism (Alkaptonuria,   Phenylketonuria, Lysosomal storage disease)   Galactosemia.   4. Autosomal dominant inheritance Adult polycystic kidney Neurofibromatosis   Marfan's syndrome (long thin extremities, ectopia lentis, aortic aneurysm)   Osteogenesis imperfecta Familial hypercholesteremia   A chondrodysplasia and familial polyposis coli.

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