Microcephaly with or without Chorioretinopathy, Lymphedema, or Intellectual Disability (MCLID)

Sponsored diagnostic testing programs for Microcephaly with or without Chorioretinopathy, Lymphedema, or Intellectual Disability (MCLID)

MCLID is a spectrum of disorders characterized by congenital microcephaly with variable chorioretinopathy, lymphedema, and intellectual disability. Presentation ranges from isolated microcephaly to multisystem involvement. Genetic testing identifies the subtype and guides management and counseling.

1 program found for Microcephaly with or without Chorioretinopathy, Lymphedema, or Intellectual Disability (MCLID)

Programs

1 program
Invitae Unlock™

Invitae Inherited Retinal Disorders Panel

This program offers U.S. clinicians access to comprehensive genetic testing for patients with suspected inherited retinal diseases, including RP, CRD, LCA, Stargardt disease, and other IRDs. Testing is also appropriate for asymptomatic individuals with a family history of IRD or a known pathogenic variant in a relevant gene, supporting diagnosis, risk assessment, and patient management.

Ophthalmology
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Performing labInvitae | Labcorp