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Sotos syndrome in two children from India.
Panigrahi, Inusha; Chaudhry, Chakshu.
Affiliation
  • Panigrahi I; Genetic Metabolic Unit, Department of Pediatrics, APC, PGIMER, Chandigarh, India.
  • Chaudhry C; Genetic Metabolic Unit, Department of Pediatrics, APC, PGIMER, Chandigarh, India.
Am J Med Genet A ; 182(9): 2181-2183, 2020 09.
Article in En | MEDLINE | ID: mdl-32677741
Sotos syndrome is one of the overgrowth syndromes, and can present with intellectual disability, behavioral problems and tall stature. In some cases, seizures, pectus deformity, cardiac and renal anomalies may be identified. Here we report two Indian children with Sotos syndrome whose initial presentation was macrocephaly and behavioral problems, respectively. The pathogenic variants in NSD1 gene were confirmed by next generation sequencing. The gene variants in the two children, one male and one female; were NSD1: c.2362C>T and NSD1: c.5474dup, respectively, leading to premature termination of protein formation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Histone-Lysine N-Methyltransferase / Sotos Syndrome / Intellectual Disability Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: India Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Histone-Lysine N-Methyltransferase / Sotos Syndrome / Intellectual Disability Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: India Country of publication: United States