Dwarfism 2
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This document discusses achondroplasia, the most common type of dwarfism. It is caused by a mutation in the FGFR3 gene which regulates bone growth. People with achondroplasia have short stature, large head, short arms and legs, bowed legs, and other skeletal abnormalities. The condition is inherited in an autosomal dominant pattern and is caused by mutations in the Fibroblast Growth Factor Receptor 3 gene which affects bone and brain development.
Dwarfism 2
- 1. DWARFISM (ACHONDROPLASIA) Gatbonton, Sharmhaine DMD 2D Parrocha, Dinah
- 2. ACHONDROPLASIA Literally means “without cartilage formation” Most common type of dwarfism. Caused by mutation of gene for (FGFR3) Average height is about 4 ft. Short arms and legs. Large head.
- 3. SIGNS AND SYMTOMS Abnormal hand appearance with persistent space between the long and ring fingers Bowed legs Decreased muscle tone Disproportionately large head-to-body size difference Prominent forehead
- 4. Shortened arms and legs (especially the upper arm and thigh) Short stature (significantly below the average height for a person of the same age and sex) Spinal stenosis Spine curvatures called kyphosis and lordosis
- 5. PATHOGENESIS The gene affected is the Fibroblast Growth Factor Receptor 3 Gene. Achondroplasia gene was mapped near the telomere of the short arm of chromosome 4. The FGFR3 protein is involved in the development and maintainance of bone and brain tissue. Receptor regulates bone growth by limiting the formation of bone from cartilage in the long bones.
- 7. DENTAL CORRELATION The administration of thyroid hormone is known to accelerate dental development and eruption. his dental development is still extremely retarded and is following a disturbed pattern in which various stages of dental development are present simultaneously.
- 8. For example, he shows absence of resorption of the deciduous canine and deciduous molar roots, which is found in children from the age of 8 onward. The permanent second molars, which usually are erupted at the age of 12 years, are still unerupted and have cortical bone overlying their occlusal surfaces. This is usually not found after the age of 12 years. To the contrary, the third molars are located in the body of the mandible, which is not frequently seen before the age of 15 years.
- 9. MENDELIAN It is inherited as a mendelian autosomal dominant trait with complete penetrance. Approximately 80% of cases are due to new or de novo dominant mutations with a mutation rate estimated to be 0.000014 per gamete per generation.
- 10. SINGLE GENE It is single gene because it only affects the Fibroblast Growth Factor Receptor 3 Gene which is responsible for the maintenace of bone and brain tissue.