Question

Achondroplasia

31 Jan 2026
Answer :
Word Count : 230
Achondroplasia is a genetic disorder characterized by dwarfism, specifically short stature due to the abnormal development of cartilage, which leads to disproportionately short limbs. It is caused by a mutation in the FGFR3 (fibroblast growth factor receptor 3) gene, located on chromosome 4. This mutation results in the activation of the FGFR3 gene, which negatively affects cartilage formation and bone growth, particularly in the long bones. The disorder follows an autosomal dominant inheritance pattern, meaning that
_________ ________ _________ _________ _______ ________ ____ _________ _______ ____ ______.
_______ ________ ______ _______ _______ _____ ____ ________ ______ ____ ____.
__________ ____ ________ _____ ______ _______ _____ ________ _______.
__________ _____ _____ _____ _____ ____ __________ ___ _______.
_______ ________ ___ __________ ________ _______ ____ _________ __________ _______ __________.
__________ _____ ______ ______ ________ _________ ______ ____ _______ __________ ________.
_______ _____ _______ _________ ___ ____ ___ ____ ___.
_______ ___ ____ ____ ____ __________ ______ _________ _______ _______.
_______ _____ _________ _________ __________ ____ _______ _______ ____ _____.
_____ ___ _____ ______ _____ ________ ____ _______ ____ ________ _______.
________ _______ __________ _________ ________ __________.
________ __________ __________ _____ ___.
________ ____ ____ __________ _______ ____ ________ ______ _________ _____ ____ ___.
___ _______ ________ ______ ______ _________.
_____ ____ _________ ______ _______.
_____ ________ ____ ___ ____.
_________ ______ __________ _____ _______ _________ ______ ____ _____ _________ __________ _________.
___.
IGNOU ACADEMY
Your IGNOU journey, made easier.
  • Solved Assignments
  • Study Notes
  • Guess Papers
  • Question Papers
Skip in 10
Top
📞
Call Support Instant phone assistance IGNOU BBCET 145 2026 - Achondroplasia | IGNOU Academy
→
🟢
WhatsApp Chat Fast live messaging
→
Email Us Business enquiries & support
→