Invitae offers chromosomal microarray analysis (CMA) as well as karyotype (routine chromosome analysis) to determine whether a developmental disorder is caused by a chromosome abnormality.
* Testing for Fragile X syndrome may be ordered with either CMA or karyotype.
* Buccal swab samples are accepted for both CMA and Fragile X testing.

Developmental Disorders (Cytogenetics)

Genetic testing for chromosomal abnormalities.

Invitae Chromosomal Microarray Analysis (CMA)

Parental or Familial Follow-up (Cytogenetics)

Familial Follow-Up for Developmental Disorders

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Invitae offers a variety of cytogenetic panels for clinicians. These panels aid in chromosome analysis for detection of specific developmental disorders.

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Cytogenetics: Genetic testing for developmental disorders

Invitae offers a variety of cytogenetic testing options for developmental disorders. Neurodevelopmental disorders (NDDs) are highly heterogeneous. Cytogenetic testing can help determines the genetic etiology of the disorder, informs prognosis, management and guides counseling of at-risk relatives.

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Developmental disorders (cytogenetics)

Invitae Chromosomal Microarray Analysis (CMA)

Invitae Chromosomal Microarray Analysis (CMA)