Your browser doesn't support javascript.
loading
An Indian child with Coats plus syndrome due to mutations in STN1.
Passi, Gouri Rao; Shamim, Uzma; Rathore, Surabhi; Joshi, Aditi; Mathur, Aradhana; Parveen, Shaista; Sharma, Pooja; Crow, Yanick J; Faruq, Mohammed.
Afiliación
  • Passi GR; Department of Pediatrics, Choithram Hospital & Research Centre, Indore, India.
  • Shamim U; Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Rathore S; Computational Structural Biology Lab, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Joshi A; Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Mathur A; Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Parveen S; Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Sharma P; Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
  • Crow YJ; Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine, Paris, France.
  • Faruq M; Centre for Genomic and Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Am J Med Genet A ; 182(9): 2139-2144, 2020 09.
Article en En | MEDLINE | ID: mdl-32627942
The role of the CTC1-STN1-TEN1 (CST) complex in Coats plus syndrome (CP), as well as other telomeropathy-phenotypes and disorders of genome instability is well documented. We report an Indian child with a clinical diagnosis of CP who presented to us with retinal exudates, extensive cerebral calcification, developmental delay and severe anemia consequent upon chronic gastrointestinal (GI) bleeding. Whole exome sequencing revealed compound heterozygous variants in STN1 as the probable genetic cause leading to CP in the present case. Of the two variants, the nonsense variant c.397C>T (p.Arg133*) was a truncating variant leading to loss of full protein length whereas the second variant c.985G>C (p.Ala329Pro) was novel and neither reported in ExAC, 1KGP or gnomAD. The deleteriousness of the novel variant was explored through molecular dynamics simulation analysis where p.Ala329Pro mutation affected C-terminal domain interaction between STN1 and TEN1 complex. Hormonal therapy using ethinyl estradiol and norethisterone was apparently associated with a clinically useful, although poorly sustained, decrease in blood transfusion requirement in the proband.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Ataxia / Convulsiones / Neoplasias Encefálicas / Calcinosis / Quistes del Sistema Nervioso Central / Proteínas de Unión a Telómeros / Leucoencefalopatías / Espasticidad Muscular Límite: Female / Humans / Infant Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Ataxia / Convulsiones / Neoplasias Encefálicas / Calcinosis / Quistes del Sistema Nervioso Central / Proteínas de Unión a Telómeros / Leucoencefalopatías / Espasticidad Muscular Límite: Female / Humans / Infant Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos