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Cornelia de Lange syndrome - Wikipedia
Cornelia de Lange's patients were two girls with unusual facies and mental retardation—one 17 months and the other 6 months—who were admitted …
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Cornelia de Lange syndrome | About the Disease | GARD
Cornelia de Lange syndrome (CdLS) is a developmental disorder that affects many parts of the body. The severity of the condition and the associated signs and symptoms can vary widely, …
Cornelia de Lange Syndrome
Learn about Cornelia de Lange Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to …
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Cornelia de Lange Syndrome - StatPearls - NCBI Bookshelf
2023年6月4日 · Cornelia de Lange syndrome (CdLS) was initially described in 1933. CdLS is a genetic disorder that affects many organs, leading to various clinical presentations. Typical …
- 作者: Marco Cascella, Maria Rosaria Muzio
- 已发布: 2023/06/04
- Publish Year: 2021
Cornelia de Lange Syndrome - Children's Hospital of …
Cornelia de Lange syndrome (CdLS) is a genetic condition present at birth. It’s characterized by numerous physical, intellectual and behavioral differences. Children with CdLS usually have low birth weight, are smaller in size and …
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Cornelia de Lange Syndrome (CdLS) - Boston Children's Hospital
Cornelia de Lange syndrome (CdLS) is a rare genetic condition that affects growth and development and can range from mild to severe. A child’s growth before and after birth is often …
Cranofacial anomalies – Cornelia de Lange Syndrome
Cornelia de Lange Syndrome is also sometimes referred to as CdLS for short or Brachman de Lange Syndrome. What does Cornelia de Lange Syndrome mean for a child? Cornelia de …
Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf
2005年9月16日 · Cornelia de Lange syndrome (CdLS) encompasses a spectrum of findings from mild to severe. Severe (classic) CdLS is characterized by distinctive facial features, growth …
Advancing the Clinical and Molecular Understanding of Cornelia …
Cornelia de Lange syndrome (CdLS) is a complex genetic disorder with distinct facial features, growth limitations, and limb anomalies. Its broad clinical spectrum presents significant …
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