Answer: 96040, Q99.2 are the codes for CPT and ICD-10-CM respectively.
Explanation:
Fragile X syndrome, also known as Martin-Bell syndrome is a genetic condition which causes developmental problems including cognitive impairment and intellectual disabilites especially among boys.
Individuals affected usually have delayed development of speech and language by age 2.
Q99.2 is a billable ICD code detailed enough for the diagnosis of fragile X chromosome. So in the ICD-10-CM Alphabetic Index , we look for Fragile X which takes us to Q99.2.
The Current Procedural Terminology (CPT) code for Fragile X syndrome as maintained by American Medical Association, is 96040. This is a medical procedural code under the range of Medical Genetics and Genetic Counseling services.
Every cell in your body has the same genes/DNA but, the gene expression process decides which genes are active in which cells which is how each cell type gets it properties.
At the heart of the eukaryotic cell-division cycle are the precise duplication and segregation of chromosomal DNA. These two events take place at distinct points of the cell cycle: DNA is replicated during S phase, and then the replicated DNA strands are accurately partitioned to the two daughter cells during M phase.
Answer:
They have all been made stronger by surviving a major life change.
Explanation:
That just doesn't seem logical without resilience
If there is an option for Vitamin B12 then that will be your answer.
