In through the nose and out through the mouth!
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.
The brain region that plays a key role in integrating information and sending appropriate signals to autonomic centers is the amygdala. The amygdala receives sensory information from multiple pathways.
The amygdala, also known as the 'fear center' is located in the medial temporal lobe.
The amygdala receives sensory information from subcortical and cortical processing pathways, which is associated with the threat, and then orchestrates reactions by controlling the autonomic center.
The amygdala is involved in the perception of different emotions (e.g., anger, fear, sadness, etc).
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