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Results 1 - 9 of 9 for "Smith-Lemli-Opitz" syndrome
  1. Smith-Lemli-Opitz syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by distinctive facial features, ...
  2. ... bile acids). More than 200 mutations that cause Smith-Lemli-Opitz syndrome have been identified in the DHCR7 gene. Smith-Lemli-Opitz syndrome is a developmental disorder characterized by distinctive facial ...
  3. ... polydactyly Laurence-Moon-Biedl syndrome Rubinstein-Taybi syndrome Smith-Lemli-Opitz syndrome Trisomy 13
  4. ... Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome Smith-Lemli-Opitz syndrome Use of the medicine hydantoin (phenytoin) during pregnancy ( ...
  5. ... Beckwith-Wiedemann syndrome Potter syndrome Rubinstein-Taybi syndrome Smith-Lemli-Opitz syndrome Treacher Collins syndrome Trisomy 13 Trisomy 18
  6. ... Robin syndrome Progeria Russell-Silver syndrome Seckel syndrome Smith-Lemli-Opitz syndrome Treacher-Collins syndrome Trisomy 13 Trisomy 18 XO ...
  7. ... syndrome Down syndrome Rubinstein-Taybi syndrome Seckel syndrome Smith-Lemli-Opitz syndrome Trisomy 18 Trisomy 21 Other problems that may ...
  8. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
  9. Lipid Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...