Hey!!
Mention any two autosomal genetic disorders with their symptoms.
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1) sickle cell anemia
2) phenylketonuria
Above mentioned both disorders are autosomal genetic disorders.
In sickle cell anemia, there is change in shape of red blood cells i.e. normal shape of RBC is biconcave which changes to sickle shaped. There is paleness on face, conjunctiva, nails etc, weakness, etc are some symptoms for the same disorder.
In phenylketonuria, there is deficiency of a digestive enzyme called phenylalanine hydroxylases. Delay in development of body, brain damage, loss of skin colour, etc are some symptoms for the same disorder.
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