A nurse can
identify possible developmental dysplasia of the hip (DDH) during a newborn
assessment through asymmetry of the gluteal folds. Asymmetrical buttock creases can
suggest hip dysplasia in infants but an ultrasound or x-ray study will need to
be done to determine whether the hips are normal or not just like a hip click.
<span>If the PH and temperature changed significantly beyond the enzyme optimum level it will become denatured and then the enzyme would not work.
The Enzyme is a biological catalyst which speeds up a reaction. The Enzyme has molecules which act upon as substrates and then it converts those substrates into different molecules which are called products.
The study of the enzyme is known as enzymology, and they are well known to catalyze more than 5,000 biochemical reaction types.</span>
1. The strength of magnetic field at A is 64 unit, then the magnetic field strength at B. is 256 units.
64 × 64 = 256 units.
2. If the strength of magnetic field B is 6 units then the strength magnetic field at A is 24 units.
which is 256 : 4 = 16 units.
Magnetic field is one of the two ways where the intensity of magnetic field is being expressed.
They feed by filtering feeding they feed on tiny organic material which is filtered through them
The disorder where the grandfather and the grandchild are affected is related with the X chromosome and is called Sex linked or X linked disorder.
<h3><u>Explanation:</u></h3>
All the sex linked disorders are recessive in character i.e the normal allele is dominant over the mutated allele. In females, there are 2 X chromosomes, so the mutated allele is only expressed when there are both the mutated alleles, else its masked by the dominant normal allele. But in males, there's only one X chromosome, so if a mutated allele is present, it's readily expressed.
If the Grandfather is diseased, then he must have that mutated allele in X chromosome. Through reproduction, its received by the mother, but she is normal because the other allele received from grandmother was normal. But mother has one of the X chromosomes with mutated allele, which is received by the grandson who again becomes diseased.
So the disorder must be X linked disorder
