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10:08
YouTube
JJ Medicine
Albinism | Genetics, Different Types, and What You Need to Know
Lesson on Albinism. The genetic condition known as albinism is more aptly known as oculocutaneous albinism due to its ocular and cutaneous manifestations. An individual with albinism is colloquially known as an “albino”. Oculocutaneous albinism is a group of rare genetic conditions of melanin biosynthesis, with a total of 7 different ...
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SOLVED: OnAlbinism is a recessive autosomal genetic disorder that causes the complete or partial absence of pigments in the skin, hair, and eyes. Fill in the Punnett square and determine the expected genotypic ratios from crossing homozygous recessive and heterozygous dominant parents.Genotypes:Genotypic Ratio:Phenotypes:% of kids with disorder:% of carrier kids:A normal male and a female who is a carrier for colorblindness. XH XH Xh Genotypes:Y% of kids with disorder:Circle their gender(s) male
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SOLVED:Albinism in humans is inherited as a simple recessive trait. Determine the genotypes of the parents and offspring for the following families. When two alternative genotypes are possible, list both. (a) Two parents without albinism have five children, four without albinism and one with albinism. (b) A male without albinism and a female with albinism have six children, all without albinism.
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SOLVED: Two couples are heterozygous for genes that cause albinism; but each gene specifies a different enzyme in the biochemical pathway for skin pigment synthesis. Their children, thus, do not face a 25% risk of having albinism: AnswerClara has severe neurofibromatosis type She has brown spots on her skin and several large tumors beneath her skin. A gene test shows that her son has inherited the disease-causing autosomal dominant allele, but he has no symptomsAnswerMateo, an apparently healthy
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