BRWD3, CDKN1C, CUL4B, DNMT3A, EED, EZH2, GLI3, GPC3, MED12, NFIX, NSD1, PHF6, PTCH1, PTEN, RNF135, UPF3B
Overgrowth/Macrocephaly NGS Panel
Overgrowth/Macrocephaly NGS Panel
The Overgrowth/Macrocephaly NGS Panel is a 16-gene panel intended for patients with a diagnosis or clinical suspicion of an overgrowth syndrome or macrocephaly.
Bannayan-Riley-Ruvalcaba syndrome, Cowden syndrome, Syndromic autism, Borjeson-Forssman-Lehmann syndrome, Cowden syndrome, FG syndrome, Greig cephalopolysyndactyly syndrome, Lujan-Fryns Syndrome, Malan overgrowth syndrome, Marshall-Smith syndrome, Simpson-Golabi-Behmel syndrome, Sotos syndrome, Tatton-Brown-Rahman syndrome, Weaver syndrome, X-linked intellectual disability with marfanoid habitus
Clinical Information
This panel consists of 16 genes associated with various syndromic forms of overgrowth and macrocephaly due to germline variants. Many of these disorders can present similarly making it difficult to pinpoint the specific diagnosis. Overgrowth may be present in neonates at birth or develop at a later age. In some cases, the patient’s growth may normalize as they get older. Additional features for many of the conditions on the panel include intellectual disability, congenital anomalies, or an increased risk for tumors.
Technical Information
This panel is performed by Next Generation Sequencing and covers the coding regions of the listed genes and the flanking intronic sequences. Promoter, 3′ untranslated sequences, and deep intronic sequences are also covered, but only known disease-causing variants in these regions will be reported. Variants identified on the panel are confirmed with Sanger sequencing if they do not meet certain quality thresholds.
Large deletions and duplications (CNVs) affecting the genes of the panel can be detected; however, due to defined settings in the analysis software, CNVs smaller than 2-kb may not be identified (for example, some small exonic level copy number changes may not be identified). Please note that certain types of genetic alterations including trinucleotide repeat expansions, methylation abnormalities, and balanced rearrangements (e.g., inversions, reciprocal translocations) may not be detected by the current analysis.
Specimen Requirements
Transport Instructions
Connect With Our Experts
Call 1-800-473-9411 to speak with our team of laboratory genetic counselors for questions or additional information.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC
