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Results 1 - 10 of 10 for Sotos syndrome
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  1. Sotos syndrome 
    Sotos syndrome is a disorder characterized by a distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development of ...
    https://medlineplus.gov/genetics/condition/sotos-syndrome - Genetics
  2. 19p13.13 deletion syndrome 
    ... 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( ...
    https://medlineplus.gov/genetics/condition/19p1313-deletion-syndrome - Genetics
  3. NSD1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/nsd1 - Genetics
  4. 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 ...
    https://medlineplus.gov/growthdisorders.html - Health Topics
  5. Natal teeth 
    ... Hallermann-Streiff syndrome Cleft palate Pierre-Robin syndrome Soto syndrome
    https://medlineplus.gov/ency/article/003268.htm - Medical Encyclopedia
  6. 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 ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
  7. Large-for-Gestational-Age (LGA) Newborns (Merck & Co., Inc.)  
    birthweight,birth weight,macrosomia,Sotos,Beckwith,Wiedemann,Wiedeman,LGA infant,LGA newborn,large for gestational age,gestational age
    https://www.merckmanuals.com/...arge-for-gestational-age-lga-newborn - External Health Links
  8. Coffin-Lowry syndrome 
    ... 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): ...
    https://medlineplus.gov/genetics/condition/coffin-lowry-syndrome - Genetics
  9. KCNQ1 gene 
    ... 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( ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  10. DCTN1 gene 
    ... Citation on PubMed Vilarino-Guell C, Wider C, Soto-Ortolaza ... the genetics and pathology of Perry syndrome. J Neurol Sci. 2010 Feb 15;289(1- ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics