International Journal For Multidisciplinary Research

E-ISSN: 2582-2160     Impact Factor: 9.24

A Widely Indexed Open Access Peer Reviewed Multidisciplinary Bi-monthly Scholarly International Journal

Call for Paper Volume 6 Issue 1 January-February 2024 Submit your research before last 3 days of February to publish your research paper in the issue of January-February.

Achrodogenesis is Disease of Cartilage Gene Defect and Skeletal Phenotype of Baby

Author(s) Kishor Nivrutti Deshmukh, Jagruti Ravindra Patil, Shubham Prabhakar Chavan, Dinesh Ravindra Pawar
Country India
Abstract Achondrogenesis group OF Serve affect is a disorders that Cartilage and ment. It is dypalsia, bone develop-type of Skeletal Charecterised by the babis and Small Children's the developent and growth of organ's It Includes, extreme Short trunk and Small growth of in approximately births are Stops micromidia ungrowth and orgens- 40,000+ live. Achrododonogesis Classified into the two subclass. type IB and Type -2 Clinical & radiological histologicul LA based mainly Gerietarea Features. The disease when Zygote is produced with only genes. Occring a pare paternal nuclear. Standard Sextual reproduction One female and one make parent each produce gametes & Gromosomes
Keywords Achrododonogesis, Achromatopsia, Skeleton disorder, Genetic background, Clinical manifestation, Gene replacement therapy.
Field Medical / Pharmacy
Published In Volume 6, Issue 1, January-February 2024
Published On 2024-02-05
Cite This Achrodogenesis is Disease of Cartilage Gene Defect and Skeletal Phenotype of Baby - Kishor Nivrutti Deshmukh, Jagruti Ravindra Patil, Shubham Prabhakar Chavan, Dinesh Ravindra Pawar - IJFMR Volume 6, Issue 1, January-February 2024. DOI 10.36948/ijfmr.2024.v06i01.12970
DOI https://doi.org/10.36948/ijfmr.2024.v06i01.12970
Short DOI https://doi.org/gtg6qz

Share this