Which one is a hereditary disease? (a) Cataract (b) Leprosy (c) Blindness (d) Phenylketonuria

Which one is a hereditary disease?
(a) Cataract (b) Leprosy
(c) Blindness (d) Phenylketonuria
by

1 Answer

Answer :

(d) Phenylketonuria
by

Related questions

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Consider the following human diseases: 1. Anaemia 2. Haemophilia 3. Leukemia 4. Phenylketonuria Which of the above diseases are hereditary in nature? (a) 1, 2 and 3 (b) 1 and 4 (c) 2 and 3 (d) 2 and 4

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A polygenic inheritance in human beings is (a) skin colour (b) phenylketonuria (c) colour blindness (d) sickle cell anaemia

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Increased urinary indole acetic acid is diagnostic of (A) Maple syrup urine disease (B) Hartnup disease (C) Homocystinuia (D) Phenylketonuria

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Phenylketonuria?

Description : Phenylketonuria?

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Tricorrhexis nodosa is a characteristic finding of (A) Argininosuccinic aciduria (B) Citrullinemia (C) Phenylketonuria (D) Hyperargininemia

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Amount of phenylacetic acid excreted in the urine in phenylketonuria is (A) 100–200 mg/dL (B) 200–280 mg/dL (C) 290–550 mg/dL (D) 600–750 mg/dL

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Absence of phenylalanine hydroxylase causes (A) Neonatal tyrosinemia (B) Phenylketonuria (C) Primary hyperoxaluria (D) Albinism

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All the following are true about phenylketonuria except (A) Deficiency of phenylalanine hydroxylase (B) Mental retardation (C) Increased urinary excretion of p-hydroxyphenyl pyruvic acid (D) Decrease serotonin formation

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All the following statements about phenylketonuria are correct except (A) Phenylalanine cannot be converted into tyrosine (B) Urinary excretion of phenylpyruvate and phenyllactate is increased (C) It can be controlled by giving a lowphenylalanine diet (D) It leads to decreased synthesis of thyroid hormones, catecholamines and melanin

Description : All the following statements about phenylketonuria are correct except (A) Phenylalanine cannot be converted into tyrosine (B) Urinary excretion of phenylpyruvate and phenyllactate is increased (C) It ... diet (D) It leads to decreased synthesis of thyroid hormones, catecholamines and melanin

Last Answer : Answer : D

Which of the following has a known association with phenylketonuria? 1) Presentation in the second year of life with absence seizures. 2) The association of red hair and brown eyes. 3) Normal development. 4) Musty odour. 5) Response of some patients to piridoxine.

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Last Answer : Answers-4 Phenylketonuria is a quarter as common as congenital hypothyroidism, with an incidence of 1:10,000 live births. It is due either to phenylalanine hydroxylase deficiency or problems ... Co-factor defects are treated with a diet low in phenylalanine and high in neurotransmitter precursors.

.Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

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Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait(c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

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Last Answer : (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11