How To Use Autosomal dominant disorder In A Sentence
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Neurofibromatosis type 1 is a common autosomal dominant disorder with a high rate of penetrance. It is caused by the mutation of the tumor suppressor gene NF1, which encodes neurofibromin.
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HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
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Familial nonsyndromic craniosynostosis, which affects 2 to 6 percent of infants with sagittal synostosis and 8 to 14 percent of infants with coronal synostosis, is transmitted as an autosomal dominant disorder.
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This means that in each pregnancy, the fetus has a 50 percent chance of inheriting the autosomal dominant disorder.
Genetics and Alagille Syndrome
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Multiple osteochondromas can occur either spontaneously an autosomal dominant disorder known as hereditary multiple exostoses.
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Conclusion: EXT is an autosomal dominant disorder and the penetrance is 97 % in this report.
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Alagille syndrome is an autosomal dominant disorder, which means someone who carries the Jagged1 gene mutation has a 50 percent chance of passing on that mutation to their child.
What Causes Alagille Syndrome?