A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy. Issue 67 (June 2018)

• Record Type: Journal Article
• Authors: Liu, Yedan; Guo, Ya; Liu, Peipei; Li, Fei; Yang, Chengqing; Song, Jie; Hu, Jingfei; Xin, Dandan; Chen, Zongbo
• Is Part Of: International journal of developmental neuroscience. Issue 67(2018:Jun.)
• Page Start: 51
• Page End: 54
• Publication Date: 2018-06
• Subjects: Pitt-Hopkins syndrome -- TCF4 -- De novo -- Epilepsy; Developmental neurobiology -- Periodicals; Neurology -- Periodicals; Neurologie du développement -- Périodiques; Developmental neurobiology; Periodicals; 612.8
• DOI: 10.1016/j.ijdevneu.2018.03.010
• Languages: English
• ISSNs: 0736-5748

Abstract

Highlights: Pitt-Hopkins Syndrome (PTHS) is a rarely reported developmental disorder caused by mutations in transcription factor 4 (TCF4) gene. We described the first case of Pitt-Hopkins syndrome from mainland China in a 10-year-old girl diagnosed at molecular level. We found that the c.2182C > T (p.Arg728Ter) mutation was a de novo nonsense mutation at exon 18 in the TCF4 gene of the patient. Abstract: Pitt-Hopkins syndrome (PTHS), belonging to the group of 18q-syndromes, is a rare genetic disorder caused by mutations in TCF4. PTHS is characterized by distinctive facial appearance, intermittent hyperventilation, intellectual disability and developmental delay. Although patients with PTHS generally have various systemic symptoms, most of them with a TCF4 mutation manifest the central nervous system (CNS) disorders. We described the first Chinese case with Pitt-Hopkins syndrome based on clinical presentations and genetic findings. In addition to the typical features of PTHS, the girl also had paroxysms of tachypnea followed by cyanosis and recurrent seizures. Comprehensive medical examinations were performed including metabolic screening, hepatic and renal function evaluation, abdominal and cardiac ultrasounds. The presence of epileptic discharges in electroencephalography and abnormal brain magnetic resonance imaging were found. High-throughput sequencing was used to detect genetic mutations associated with CNS disorders. Sanger sequencing was used to confirm the mutations in the patient. The c.2182C＞T (p.Arg728Ter) mutation was a de novo nonsense mutation at exon 18 in the TCF4 gene of the patient. In conclusion, we have identified a de novo nonsense mutation of TCF4 carried by a Chinese girl with PTHS. The patient underwent anti-epileptic therapy (sodium valproate, levetiracetam, clonazepam), resulting in a reduction of the seizures.