Osteomalacia and rickets
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Osteomalacia and rickets
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Which of the following set of laboratory findings will be most likely present in this patient?
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Calcium
in osteomalacia/rickets p. 468
Hypophosphatemic rickets p. 57
Osteomalacia/rickets p. 468
Parathyroid hormone (PTH) p. 334
osteomalacia/rickets p. 468
Rachitic rosary p. 468
Rickets p. 468
Fanconi syndrome p. 725
hypophosphatemic p. 611, 611
inheritance p. 57
lab values in p. 469
vitamin D deficiency p. 68
Vitamin D deficiency p. 348
osteomalacia/rickets p. 468, 468
Transcript
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Bone softening caused by a faulty process of bone mineralization manifests as either rickets in children or osteomalacia in adults.
Inadequate bone mineralization could be due to a deficient or impaired metabolism of vitamin D, phosphate or calcium.
But first, a bit about bones. Now, long bones, like the femur, are made up of two epiphyses, which are its ends, and the diaphysis, which is the shaft.
Between each epiphysis and the diaphysis, there’s a region called the metaphysis.
And the metaphysis contains the epiphyseal plate, or the growth plate, which is the part of the bone that grows during childhood.
Once growth stops, the growth plate is replaced by an epiphyseal line, and this is known as epiphyseal closure.
Now, for bones to grow and develop properly, special bone cells, called osteoblasts, are hard at work.
To build bone, osteoblasts secrete osteoid, which is an organic matrix made of type 1 collagen.
These collagen fibers are the framework for the osteoblasts' work.
Osteoblasts then deposit calcium and phosphate crystals into the framework.
This process is called bone mineralization, and it confers strength to the growing bones.
Bone mineralization is dependent on an enzyme called alkaline phosphatase - which increases in response to osteoblast activity.
So, at the end of the day, bones are like a storage warehouse for calcium and phosphate.
Now, the levels of calcium and phosphate in the bone, but also in the blood, are regulated by vitamin D and parathyroid hormone, or PTH.
Vitamin D-wise, two steps are necessary for optimal metabolism: first, there must be enough vitamin D in the body, either from food, or created in the skin in response to sunlight exposure.
Secondly, vitamin D must become metabolically active, and this process also has two steps.
First one happens in the liver, where inactive vitamin D is converted into 25-hydroxy-vitamin D by the enzyme 25-Hydroxylase.
25-hydroxy-vitamin D then travels to the kidneys, where the enzyme 1-alpha-hydroxylase converts it to 1,25 hydroxy-vitamin D, or calcitriol, which is the active form of vitamin D.
Summary
Rickets and osteomalacia are conditions characterized by bone softening due to a calcium deficiency or lack of vitamin D. The main difference between the two is the age at which they occur. Osteomalacia affects adults, whereas rickets affects children.
The key symptoms are diffuse bone and joint pain, proximal muscle weakness, bone fragility, and increased risk of fractures with minimal trauma. For rickets, there may also be craniotabes( softening and thinning of skull bones). The treatment typically involves vitamin D supplementation and treating the underlying cause.
Sources
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- "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
- "The Developmental Basis of Skeletal Cell Differentiation and the Molecular Basis of Major Skeletal Defects" Biological Reviews (2008)
- "Triradiate deformity of the pelvis in Paget's disease of bone." Postgraduate Medical Journal (1980)
- "Vitamin D supplementation in pregnancy: a systematic review" Health Technology Assessment (2014)