A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation
Cornelia de Lange syndrome (CDLS) is caused by pathogenic variants in genes which are structural or regulatory components of the cohesin complex. The classical Cornelia de Lange (CDLS) phenotype is characterized by distinctive facial features, growth retardation, upper limb reduction defects, hirsut...
Main Authors: | Anca Maria Panaitescu, Simona Duta, Nicolae Gica, Radu Botezatu, Florina Nedelea, Gheorghe Peltecu, Alina Veduta |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-01-01
|
Series: | Diagnostics |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-4418/11/1/142 |
Similar Items
-
Cornelia de-Lange syndrome
by: Gupta D, et al.
Published: (2005-03-01) -
Behavioral phenotype and autism spectrum disorders in Cornelia de Lange syndrome
by: Lucia Parisi, et al.
Published: (2015-09-01) -
Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome
by: Fengchang Qiao, et al.
Published: (2021-02-01) -
An eighteen month-old infant with Cornelia de Lange syndrome: a case report
by: Reza saeidi, et al.
Published: (2015-12-01) -
Surgical treatment of esotropia and unilateral ptosis in a patient with Cornelia de Lange syndrome
by: Won Jae Kim
Published: (2019-05-01)