What is the Difference Between Achondroplasia and Pseudoachondroplasia?
🆚 Go to Comparative Table 🆚Achondroplasia and pseudoachondroplasia are both genetic disorders characterized by short stature and bone growth abnormalities, but they have distinct differences in their genetic causes and clinical manifestations.
Achondroplasia:
- Caused by mutations in the gene encoding fibroblast growth factor receptor 3 (FGFR3).
- Results in rhizomelic short stature, frontal bossing with midface hypoplasia, short ribs, trident hand, limited elbow extension, and other facial features.
- Inherited in an autosomal dominant pattern.
Pseudoachondroplasia:
- Caused by mutations in the gene encoding cartilage oligomeric matrix protein (COMP).
- Causes short stature, short arms and legs, skeletal abnormalities, joint laxity, and joint pain, but does not affect facial features, head size, intelligence, or lifespan.
- Inheritance can be autosomal dominant or occur randomly due to spontaneous mutations.
In summary, the main differences between achondroplasia and pseudoachondroplasia lie in their genetic causes, clinical manifestations, and inheritance patterns. While both conditions result in short stature, pseudoachondroplasia is characterized by more severe bone growth abnormalities and does not affect facial features or intelligence.
Comparative Table: Achondroplasia vs Pseudoachondroplasia
Achondroplasia and pseudoachondroplasia are both genetic disorders characterized by short stature and short-limb dwarfism. However, they have distinct differences in their causes, symptoms, and radiographic features. Here is a table comparing the two conditions:
Feature | Achondroplasia | Pseudoachondroplasia |
---|---|---|
Causative Gene | FGFR3 (Fibroblast Growth Factor Receptor 3) | COMP (Cartilage Oligomeric Matrix Protein) |
Key Symptoms | - Short stature <40" (or 43") | - Short stature <36" |
- Disproportionately short limbs | - Disproportionately short limbs | |
- Large head with frontal bossing | - Normal or slightly enlarged skull | |
- Limited elbow extension | - Moderate joint stiffness | |
Diagnostic Tests | - X-rays | - X-rays |
Both conditions are inherited as autosomal dominant disorders, meaning that an affected individual has a 50% chance of passing the condition to their offspring. Diagnosis is typically made through a comprehensive medical history, physical examination, and diagnostic tests such as X-rays. Treatment for both conditions often involves surgical interventions to address complications related to the disorders, such as spinal fusion for instability, spinal stenosis, or hip problems.
- Achondroplasia vs Hypochondroplasia
- Enchondroma vs Chondrosarcoma
- Endochondral Ossification vs Intramembranous Ossification
- Plagiocephaly vs Craniosynostosis
- Dermal vs Endochondral Ossification
- Chondroblasts vs Chondrocytes
- Synchondrosis vs Symphysis
- Dwarfism vs Cretinism
- Mesenchyme vs Ectomesenchyme
- Congenital Adrenal Hyperplasia vs Hypoplasia
- Hermaphrodite vs Pseudohermaphrodite
- Differentiation vs Morphogenesis
- Osteogenesis Imperfecta vs Osteoporosis
- Chondromalacia Patella vs Patellofemoral Pain Syndrome
- Chondrichthyes vs Osteichthyes
- Agenesis vs Atresia
- Metaplasia vs Dysplasia
- Mesoderm vs Mesenchyme
- Bone vs Cartilage