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Results 1 - 10 of 11 for "Sotos'" syndrome
  1. Sotos syndrome is a disorder characterized by a distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development of ...
  2. Sotos Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Growth Disorders/Specifics ... Growth Disorders ... National Institute of Neurological Disorders and ...
  3. ... E, Ploski R, Krajewska-Walasek M. Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion ... on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome. Am J Hum Genet. 2010 Aug 13;87( ...
  4. ... NSD1 gene have been identified in people with Sotos syndrome. The most common mutation in the Japanese population ... disabilities, and the other signs and symptoms of Sotos syndrome. More About This Health Condition A change involving ...
  5. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  6. Growth Disorders (National Library of Medicine)  
    Does your child seem much shorter - or much taller - than other kids his or her age? It could be normal. Some children may be small for their age but still be ...
  7. ... Hallermann-Streiff syndrome Cleft palate Pierre-Robin syndrome Soto syndrome
  8. birthweight,birth weight,macrosomia,Sotos,Beckwith,Wiedemann,Wiedeman,LGA infant,LGA newborn,large for gestational age,gestational age
  9. ... PubMed or Free article on PubMed Central Herrera-Soto JA, Santiago-Cornier A, Segal LS, Ramirez N, Tamai J. The musculoskeletal manifestations of the Coffin-Lowry syndrome. J Pediatr Orthop. 2007 Jan-Feb;27(1): ...
  10. ... Brugada J, Oliva A, Burashnikov E, Santos-de-Soto J, Grueso-Montero J, Diaz-Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res. 2005 Dec 1;68( ...
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