Biological Science, Loose-leaf Edition (7th Edition)
Biological Science, Loose-leaf Edition (7th Edition)
7th Edition
ISBN: 9780135272800
Author: Scott Freeman, Kim Quillin, Lizabeth Allison, Michael Black, Greg Podgorski, Emily Taylor, Jeff Carmichael
Publisher: PEARSON
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Chapter 14, Problem 22PIAT
Summary Introduction

To review:

The reason behind the occurrence of color blindness in the son without Adrenoleukodystrophy (ALD).

Introduction:

Adrenoleukodystrophy (ALD) is a type of X-linked disorder. It occurs as a result of mutation in the ABCD1 gene, which is present on the Xq28 chromosome. Furthermore, the nonfunctioning of these enzymes damages the myelin sheath present on the axon, which further causes degeneration of neuron.

A woman is heterozygous for a colorblindness allele. At a site on the chromosome with the color blindness allele, a new mutation occurs causing ALD, creating one chromosome with an allele for color blindness and an allele for ALD. Woman bears a colorblind child but does not have ALD.

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Find the dental formula and enter it in the following format: I3/3 C1/1 P4/4 M2/3 = 42 (this is not the correct number, just the correct format) Please be aware: the upper jaw is intact (all teeth are present). The bottom jaw/mandible is not intact. The front teeth should include 6 total rectangular teeth (3 on each side) and 2 total large triangular teeth (1 on each side).
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