How to Cite this Article: Gripp KW, Hopkins E, Johnston JJ, Krause C, Dobyns WB, Biesecker LG. 2011. Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene. Am J Med Genet Part A 155:2516–2520.
Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene†
Article first published online: 9 SEP 2011
Copyright © 2011 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 10, pages 2516–2520, October 2011
How to Cite
Gripp, K. W., Hopkins, E., Johnston, J. J., Krause, C., Dobyns, W. B. and Biesecker, L. G. (2011), Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene. Am. J. Med. Genet., 155: 2516–2520. doi: 10.1002/ajmg.a.34190
- Issue published online: 20 SEP 2011
- Article first published online: 9 SEP 2011
- Manuscript Accepted: 1 JUN 2011
- Manuscript Received: 23 MAY 2011
- Intramural Program of the National Human Genome Research Institute of the National Institutes of Health
- persistent left superior vena cava;
- Pierre–Robin sequence;
- talipes equinovarus;
TARP syndrome, comprising Talipes equinovarus, atrial septal defect (ASD), Robin sequence (micrognathia, glossoptosis, and cleft palate), and persistence of the left superior vena cava, is an X-linked condition with pre- or postnatal lethality in affected males. Based on linkage studies and massively parallel sequencing of X-chromosome exons in two families, the disease-causing gene was identified as RBM10. We identified a maternally inherited frameshift mutation in an unrelated patient, confirming RBM10 as the disease gene. This is the first reported individual with TARP syndrome who survived past early infancy, thus expanding the phenotypic spectrum of this disorder. In addition to the characteristic cleft palate, ASD, and persistent superior vena cava, he had low-set and posteriorly angulated ears, upslanting palpebral fissures, cryptorchidism, and structural brain abnormalities including partial agenesis of the corpus callosum, dysplastic enlarged caudate, and cerebellar hypoplasia with megacisterna magna. Preterm delivery, suspected pulmonary hypoplasia, and pulmonary hypertension resulted in chronic lung disease. At the age of years, he remained ventilator-dependent at night, and he was fed exclusively through a gastro-jejunal tube. Sensorineural hearing loss required a hearing aid. Optic atrophy and cortical visual impairment were noted. He was unable to sit independently, was non-communicative and he had severe intellectual disability. Atrial flutter required recurrent ablation of intra-atrial re-entry pathways. The mother's heterozygosity for the RBM10 mutation underscored the importance of accurate diagnosis and counseling for TARP syndrome. © 2011 Wiley-Liss, Inc.