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Results 1 - 8 of 8 for Congenital muscular "hypertrophy-cerebral" syndrome
  1. Genetics Home Reference: Cornelia de Lange syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Genetic testing OMIM Genetic disorder catalog Conditions > Cornelia de Lange syndrome On this page: Description Genetic changes Inheritance Diagnosis ... Glossary definitions Reviewed July 2012 What is Cornelia de Lange syndrome? Cornelia de Lange syndrome is a developmental disorder ...
  2. Cornelia de Lange Syndrome Foundation (Cornelia de Lange Syndrome Foundation)  
    ... Outside Links Privacy & Terms Site Map The Cornelia de Lange Syndrome (CdLS) Foundation is a family support organization that ...
  3. Characteristics of CdLS (Cornelia de Lange Syndrome) (Cornelia de Lange Syndrome Foundation)  
    Characteristics of CdLS As with many other syndromes, individuals with CdLS strongly resemble one another. Typical facial features include thin eyebrows that meet in ...
  4. ... rare causes include: Apert syndrome Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome Smith-Lemli-Opitz syndrome Use of ...
  5. Birth Defects (National Library of Medicine)  
    A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. ...
  6. Oculomotor Apraxia (American Association for Pediatric Ophthalmology and Strabismus)  
    ... vermis astrocytoma, vermis cyst, carotid fibromuscular hypoplasia, Cornelia de Lange syndrome, and microphthalmos. What causes OMA to develop? The ...
  7. ... malnutrition. Genetic conditions that cause microcephaly include: Cornelia de Lange syndrome Cri du chat syndrome Down syndrome Rubinstein-Taybi ...
  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 disorders. Or ...