Achondroplasia
An autosomal dominant disorder caused by mutation(s) in the FGFR3 gene, encoding fibroblast growth factor receptor 3. The condition is characterized by inappropriate cartilage growth plate differentiation and deficient endochondral growth, manifest clinically with severe rhizomelic short stature, short limbs, characteristic facies with frontal bossing and midface hypoplasia.
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thanks for the interest, comments and your contribution to this case of achondroplasia.lt has enlightened me.
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THE CONCLUSION OF THE CASE OF KERSTACONUS IS THAT WE AS OPHTHALMOLOGISTS SHOULD KNOW WHOLE SCENERIO OF KERSTACONUS THAT IS WHAT ARE MEDICAL CONDITIONS ASSOCIATED WITH THIS DISORDER AND WHST ARE OPHTHALMIC CONDITION ASDOCIATIONS HERE I HAVE...
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Metaphyseal flaring of femur and tibia. Long fibula-the fibular head present at the level of tibial plateau. Characteristic features of achondroplasia.
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Recent Cases of Achondroplasia
Browse recently discussed Achondroplasia cases by specialistsTop Cases of Achondroplasia
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Top Achondroplasia Doctors on Curofy
Top doctors who continously share their opinions on AchondroplasiaFlorence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
Sangrur
Distt.Immunization Officer
Guru Gobind Singh Govt. Medical College, Faridkot
MBBS,DCH
National Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics
Self Employed. Now Doing My Practice
Pediatric Consultant
MKCG MCH
MBBS and MD (pediatrics)
VSS.MEDICAL COLLEGE & HOSPITALS.
Professor Radiology. 1984 To 1993 Superintendent & Principal. 93 To 96 Director Medical Education.96 To 98.
Patna Medical College.
MD
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