Collect whole blood in a purple top (EDTA) tube.
Refrigerate sample until shipment. Send the sample at room temperature with overnight delivery for receipt Monday through Friday within 24 hours of collection.
Whole blood can be refrigerated until shipment.
Heparinized specimens, severely hemolyzed specimens, frozen, clotted or possibly commingled specimens, blood in non-sterile or leaky containers, mislabeled or inappropriately labeled specimens.
Do not heat, freeze or centrifuge blood before shipment. Refrigerate sample until shipment.
Mon - Fri 9:00am to 4:00pm
81479 x 2
Pitt Hopkins Syndrome (PTHS) is characterized by severe mental retardation, deep set eyes, broad and beaked nasal bridge, wide mouth, cupid’s bow upper lip, a protruding lower face and intermittent hyperventilation followed by apnea. In addition, patients can show a happy personality, stereotypic movements which in addition to microcephaly, breathing anomalies, mental retardation and seizures resemble the features seen in both Rett and Angelman syndromes. Hirschsprung disease and constipation overlap with features observed in Mowat-Wilson syndrome.
TCF4 is located on chromosome 18q21.2 and it encodes a member of the bHLH transcription factor family. Missense, splice site, nonsense and large deletions have been identified in the TCF4 gene (Zweier et al. 2007, Zweier et al. 2008).
We offer deletion/duplication analysis and DNA sequence analysis of the entire coding region of the TCF4 gene (exons 2-19) including splice junctions. PCR amplification and sequencing is performed on all coding exons. The patient’s gene sequence is then compared to a reference sequence. Sequence variants are classified as mutations, variants of unknown significance or benign variants unrelated to disease. Variants of unknown significance may warrant further studies in the patient and other family members.
Point mutations in TCF4 were identified in 14-35% of patients with severe mental retardation and clinical findings overlapping with PTHS (Zweier et al. 2008; De Pontual et al. 2009) while deletions have been detected in 13% of patients initially evaluated for Angelman, Mowat-Wilson, or Rett syndrome whose phenotype overlapped PHS (Giurgea et al. 2008).
de Pontual., Hum Mutat. 2009 Apr;30(4):669-76
Giurgea et al. Hum Mutat. 2008 Nov;29(11):E242-51.
Zweier et al., Am J Hum Genet. 2007 May; 80(5): 994–1001
Zweier et al ., J Med Genet. 2008 Nov;45(11):738-44
Sequence and deletion/duplication analysis of MECP2, CDKL5, FOXG1, and UBE3A. Sequence analysis of SLC9A6. Methylation-sensitive PCR for Angelman Syndrome.
Test results with interpretation will be mailed and/or faxed to the referring physician or laboratory following completion of the test. Additional reports will be provided as requested.
The clinical utility of such testing is to support a clinical diagnosis of the disease, facilitate genetic counseling, assess the risk to other first degree relatives and to facilitate testing of at - risk family members.
Whole blood in EDTA purple top tubes is the preferred sample. High molecular weight genomic DNA, cheek epithelial cells, or other samples containing DNA may be acceptable. Contact the laboratory for specific instructions regarding such samples before sending the sample.
Ask for more information about our laboratory services.