2023年7月12日 · Cornelia de Lange syndrome (CdLS) is a rare genetic condition that causes various physical, cognitive and behavioral traits. It affects many parts of your child’s body, so symptoms vary widely. The most common signs of the disorder include delayed growth and distinct facial features.

Cornelia de Lange syndrome (CdLS) is a congenital rare syndrome appear due to genetic disorders. The primary characteristic of this syndrome is delayed physical development during fetal growth and continues to after birth.

2013年11月18日 · Most of the signs and symptoms of Cornelia de Lange syndrome are visible at birth. Some of the unique facial features elicited by Cornelia de Lange syndrome patients include the following: Some of the physical symptoms which may be visible from birth or which develop as the affected child grows older include the following:

The typical features of CdLS include thick or long eyebrows, a small nose, small stature, developmental delay, long or smooth philtrum, thin upper lip and downturned mouth. [1] The syndrome is named after Dutch pediatrician Cornelia Catharina de …

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 find Patients & Caregivers

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 height and have …

2023年3月6日 · Cornelia de Lange syndrome (CdLS) is a rare genetic condition that can affect multiple organs. CdLS may cause various symptoms, including intellectual disability and characteristic facial...

Prominent facial features include thin eyebrows that often meet at the midline (synophrys), long eyelashes, short upturned nose, thin downturned lips, low-set ears, and high-arched palate or cleft palate.