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Answer: Like you said it Run in her family History.</em></h3><h3><em /></h3><h3><em>
Explanation: If when she grows up she has a (Greater chance of getting it if her side of the Has it, but if he has no symptoms right now then that doesn't mean she wont have it It might occur later as she gets older .</em></h3>
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Answer:
The symptoms involved in ontogenesis imperfect are- bone breakage, pain in bone, deformation of bones, brittle teeth, coloured tint in the white portion of eyes, loss in hearing and loose joints.
Explanation:
In the disease, ontogenesis imperfect, the strong bone formation in body is prevented by the defective gene that produces collagen protein. People who have the deficiency of collagen by birth, can develop this disease or can have it by birth. This defect can be hereditary.
The symptoms included in this disease are the- deformation and breakage of bones, pain in bone, grey or purple tint in the white portion of the eye, short stature, brittle teeth, hearing impairment and loose joints.
Under the Berlin definition, patients with PaO2/FiO2 200-300 would now have "mild ARDS." Onset of ARDS (diagnosis) must be acute, as defined as within 7 days of some defined event, which may be sepsis, pneumonia, or simply a patient's recognition of worsening respiratory symptoms.
The common monosaccharide that is found in the diet is glucose. The answer is option B. Monosaccharides are the basic components of carbohydrates. They are called simple sugars and the most common that is seen in most food is glucose. Along with glucose, other monosaccharides also include fructose and galactose.
