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Cornelia de Lange syndrome 1
Did you mean cornea de range syndrome 1?
- ... for Rare Disorders (NORD) ClinicalTrials.gov CORNELIA DE LANGE SYNDROME 1; CDLS1 CORNELIA DE LANGE SYNDROME 2; CDLS2 CORNELIA DE LANGE SYNDROME 5; ...
- ... gene have been identified in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of ... of the SMC1A gene variants that cause Cornelia de Lange syndrome change single protein building blocks (amino acids) in ...
- ... gene have been found in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of ... are the most common known cause of Cornelia de Lange syndrome, accounting for more than half of all cases. ...
- ... SMC3 gene have been found to cause Cornelia de Lange syndrome, a developmental disorder that affects many parts of ... of the SMC3 gene variants that cause Cornelia de Lange syndrome either change single protein building blocks (amino acids) ...
- ... gene have been identified in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of ... not fully understand how these changes cause Cornelia de Lange syndrome, they suspect that altered gene regulation probably underlies ...
- ... gene have been identified in people with Cornelia de Lange syndrome, a developmental disorder that affects many parts of ... cause of this condition.Some cases of Cornelia de Lange syndrome have resulted from a deletion that removes a ...
- 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. ...
- ... Registry Cooley's Anemia Foundation Corneal Dystrophy Foundation Cornelia de Lange Syndrome Foundation Costello Kids Costello Syndrome Family Network Creutzfeldt- ...
- ... rare causes include: Apert syndrome Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome Smith-Lemli-Opitz syndrome Use of ...
- ... malnutrition. Genetic conditions that cause microcephaly include: Cornelia de Lange syndrome Cri du chat syndrome Down syndrome Rubinstein-Taybi ...
