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(Solved): \begin{tabular}{|c|l|l|} \hline Genetic disorders & Causes & Phenotypic effects \\ \hline Tay-Sachs ...




\begin{tabular}{|c|l|l|}
\hline Genetic disorders & Causes & Phenotypic effects \\
\hline Tay-Sachs disease & & \\
\hline Cys
\begin{tabular}{|c|c|c|}
\hline Genetic disorders & Causes & \\
\hline Kinefelter syndrome & & Phenotypic effects \\
\hline P
\begin{tabular}{|c|l|l|} \hline Genetic disorders & Causes & Phenotypic effects \\ \hline Tay-Sachs disease & & \\ \hline Cystic fibrosis & & \\ \hline Sickle cell anemia & & \\ \hline Marfan syndrome & & \\ \hline Osteogenesis imperfecta & & \\ \hline Huntington's & & \\ \hline disease & & \\ \hline \begin{tabular}{c} Turner syndrome \\ \hline \end{tabular} & & \\ \hline \end{tabular} \begin{tabular}{|c|c|c|} \hline Genetic disorders & Causes & \\ \hline Kinefelter syndrome & & Phenotypic effects \\ \hline Poly-X-females & & \\ \hline Jacobs syndrome & & \\ \hline Wiliams syndrome & & \\ \hline \begin{tabular}{c} Down Syndrome \\ \hline Philadelphia \\ chromosome \end{tabular} & & \\ \hline Robertsonian translocation & & \\ \hline \end{tabular}


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Tays sachs disease: It is a genetic disorder caused by deficiency of hexoaminadase enzyme which is a lysosomal enzyme. It acts on N-acetylglucosamine on brain ganglioside. The symptoms are enhanced reaction to sharp sounds and a cherry coloured spot
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