Received 01/06/2023 review began 01/17/2023 review ended 01/20/2023 published 01/25/2023

HIGHLIGHTS

• who: Report et al. from the Institute of Higher Education and Research, Wardha, IND have published the research: Received 01/06/2023 Review began 01/17/2023 Review ended 01/20/2023 Published 01/25/2023, in the Journal: (JOURNAL) of January/25,/2023
• what: We presented a case of achondroplasia with bilateral developmental cataracts.

SUMMARY

Achondroplasia is an autosomal dominant congenital disorder of enchondral ossification. A mutation in the fibroblast growth factor receptor 3 (FGFR3) gene causes dysplasia of enchondral formation, which leads to the development of achondroplasia. The authors . . .

 



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