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

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