What condition is indicated by the presence of blue sclera?

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Multiple Choice

What condition is indicated by the presence of blue sclera?

Explanation:
The presence of blue sclera is characteristically associated with osteogenesis imperfecta, which is a genetic disorder that affects the bones, making them fragile and prone to fractures. This condition arises due to defects in collagen synthesis, specifically Type I collagen, which is essential for bone strength and structure. The blue appearance of the sclera in individuals with osteogenesis imperfecta is due to the thinness of the scleral tissue, allowing the underlying choroidal pigment to show through. In contrast, other conditions—such as cystic fibrosis, Marfan syndrome, and Ehlers-Danlos syndrome—do not typically present with blue sclera as a hallmark sign. While these conditions have their own distinctive features, the specific manifestation of blue sclera is closely tied to the pathological changes in collagen seen in osteogenesis imperfecta. Therefore, recognizing blue sclera can prompt further investigation into possible osteogenesis imperfecta in the patient.

The presence of blue sclera is characteristically associated with osteogenesis imperfecta, which is a genetic disorder that affects the bones, making them fragile and prone to fractures. This condition arises due to defects in collagen synthesis, specifically Type I collagen, which is essential for bone strength and structure. The blue appearance of the sclera in individuals with osteogenesis imperfecta is due to the thinness of the scleral tissue, allowing the underlying choroidal pigment to show through.

In contrast, other conditions—such as cystic fibrosis, Marfan syndrome, and Ehlers-Danlos syndrome—do not typically present with blue sclera as a hallmark sign. While these conditions have their own distinctive features, the specific manifestation of blue sclera is closely tied to the pathological changes in collagen seen in osteogenesis imperfecta. Therefore, recognizing blue sclera can prompt further investigation into possible osteogenesis imperfecta in the patient.

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