Achondroplasia
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Achondroplasia: Is a congenital genetic

Achondroplasia is a congenital genetic disorder resulting in rhizomelic dwarfism and is the most common skeletal dysplasia. It has numerous distinctive radiographic features. Epidemiology It occurs due to sporadic mutations in the majority of c... Achondroplasia is a bone growth disorder that causes disproportionate dwarfism. Dwarfism is defined as a condition of short stature as an adult. People with achondroplasia are short in stature ... Achondroplasia is a disorder of bone growth that prevents the changing of cartilage (particularly in the long bones of the arms and legs) to bone. It is characterized by dwarfism, limited range of motion at the elbows, large head size (macrocephaly), small fingers, and normal intelligence. Achondroplasia can cause health complications such as interruption of breathing (apnea), obesity, recurrent ear infections, an exaggerated inward curve of the lumbar spine (lordosis). More serious problems ... Achondroplasia is a genetic disorder that affects bone growth, leading to disproportionate dwarfism. This comprehensive guide aims to provide an in-depth understanding of achondroplasia, its causes, symptoms, diagnosis, and treatment options.

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