Chromosomal Microarray (350k) Test Cost & Procedure

Patients with unexplained aberrant phenotypes, including mental retardation, developmental delay, dysmorphic characteristics, congenital malformations, and autism, may have imbalanced chromosomal abnormalities (DNA loss and gain). Long contiguous sequences of homozygosity are also found by SNP-based arrays, which may point to a higher probability of a recessive disorder or uniparental disomy.

This test is only used to identify a variety of developmental disorders:

• Mental Irregularity
• Congenital Errors

CMA, or chromosomal microarray:

It is often employed for the investigation of developmental abnormalities. This sort of genetic testing exists. It is suitable for:

• Spectrum diseases in autism
• Mental Irregularity
• Many congenital disabilities

What does an assay look for?

It identifies chromosomal regions that have been duplicated or deleted. It could contain:

• Microdeletions
• Microduplications
• Trisomy

Dwarf Syndrome

• Homozygosity

Triploidy

• Tetraploidy

What is this test unable to detect?

• Changes at a Point
• little erasures

Minimal Replication

• symmetrical inversions

a minor relocation

Autism Spectrum Disorder: What Is It?

It is one of the specific disorders of brain development. The most widely recognised opinion regarding this disorder's causes is that it has a genetic component.

Individuals with this disease behave differently around others. They might be able to communicate well, or they might even be silent.

It typically affects kids and can last a lifetime.

They demonstrate:

• Anxiety
• Depressionhyperactivity

Symptoms noticed:

• Social Communication Issues
• Interaction Issues
• Restricted Behaviors

Congenital Mistake:

• It is a structural change that takes place at birth. Several body components are impacted. These deviations could be:
  • CFootfoot, club foot defects, neural tube defects, and cleft palate

What is mental illness?

 The person in this situation has a lower-than-average Intelligence. Like other people, he might not have access to regular brain functions.

Causes:

• The syndrome of Klinefelter
• Phenylketonuria with Down syndrome

Tay Sachs sclerosis is a disease.

• Syndrome of Laurence Moon Biedl
• Galactosemia
• Fibromyalgia X Syndrome

Symptoms:

• slow growth
• childish behaviour
• Lack of understanding
• Curiosity
• Problem-solving challenges
• Poor learning caregiving birth to
• Having trouble speaking and walking